esv3856804
- Organism: Homo sapiens
- Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:37
- Validation:Not tested
- Clinical Assertions: No
- Region Size:12,430
- Publication(s):1000 Genomes Consortium Phase 3 Integrated SV
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 352 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 358 SVs from 48 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3856804 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
esv3856804 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Zygosity | Other Calls in this Sample and Study |
---|---|---|---|---|---|---|
essv21493685 | deletion | HG01101 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,648 |
essv21493686 | deletion | HG02429 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,174 |
essv21493687 | deletion | HG02502 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,021 |
essv21493688 | deletion | HG02610 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,101 |
essv21493689 | deletion | HG02624 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,877 |
essv21493690 | deletion | HG02643 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,879 |
essv21493691 | deletion | HG02676 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,958 |
essv21493692 | deletion | HG02703 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,058 |
essv21493693 | deletion | HG02760 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,040 |
essv21493694 | deletion | HG02768 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,980 |
essv21493695 | deletion | HG02895 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,924 |
essv21493696 | deletion | HG02896 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,590 |
essv21493697 | deletion | HG03046 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,832 |
essv21493698 | deletion | HG03060 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,270 |
essv21493699 | deletion | HG03064 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,978 |
essv21493700 | deletion | HG03074 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,174 |
essv21493701 | deletion | HG03077 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,244 |
essv21493702 | deletion | HG03162 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,760 |
essv21493703 | deletion | HG03303 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,011 |
essv21493704 | deletion | HG03367 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,931 |
essv21493705 | deletion | HG03517 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,434 |
essv21493706 | deletion | HG03548 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,604 |
essv21493707 | deletion | HG03556 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,910 |
essv21493708 | deletion | HG03689 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,264 |
essv21493709 | deletion | NA18501 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,193 |
essv21493710 | deletion | NA18519 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,117 |
essv21493711 | deletion | NA18539 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,199 |
essv21493712 | deletion | NA18856 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,348 |
essv21493713 | deletion | NA18873 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,059 |
essv21493714 | deletion | NA19129 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,021 |
essv21493715 | deletion | NA19317 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,484 |
essv21493716 | deletion | NA19338 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,744 |
essv21493717 | deletion | NA19378 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,801 |
essv21493718 | deletion | NA19397 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,070 |
essv21493719 | deletion | NA19430 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,134 |
essv21493720 | deletion | NA19914 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,767 |
essv21493721 | deletion | NA20281 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,450 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv21493685 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493686 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493687 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493688 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493689 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493690 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493691 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493692 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493693 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493694 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493695 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493696 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493697 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493698 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493699 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493700 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493701 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493702 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493703 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493704 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493705 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493706 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493707 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493708 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493709 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493710 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493711 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493712 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493713 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493714 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493715 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493716 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493717 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493718 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493719 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493720 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493721 | Remapped | Perfect | NC_000009.12:g.(17 256480_17256980)_( 17269409_17269909) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 17,256,980 (-500, +0) | 17,269,409 (-0, +500) |
essv21493685 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493686 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493687 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493688 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493689 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493690 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493691 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493692 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493693 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493694 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493695 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493696 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493697 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493698 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493699 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493700 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493701 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493702 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493703 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493704 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493705 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493706 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493707 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493708 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493709 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493710 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493711 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493712 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493713 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493714 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493715 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493716 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493717 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493718 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493719 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493720 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) | ||
essv21493721 | Submitted genomic | NC_000009.11:g.(17 256478_17256978)_( 17269407_17269907) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 17,256,978 (-500, +0) | 17,269,407 (-0, +500) |