esv3875353
- 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:11,869
- 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: 276 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 276 SVs from 53 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3875353 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
esv3875353 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Zygosity | Other Calls in this Sample and Study |
---|---|---|---|---|---|---|
essv23774179 | deletion | HG00103 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,063 |
essv23774180 | deletion | HG00117 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,398 |
essv23774181 | deletion | HG00178 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,406 |
essv23774182 | deletion | HG00250 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,391 |
essv23774183 | deletion | HG00267 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,486 |
essv23774184 | deletion | HG00311 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,551 |
essv23774185 | deletion | HG00361 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,647 |
essv23774186 | deletion | HG00364 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,292 |
essv23774187 | deletion | HG00379 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,279 |
essv23774188 | deletion | HG01066 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,614 |
essv23774189 | deletion | HG01259 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,642 |
essv23774190 | deletion | HG01281 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,331 |
essv23774191 | deletion | HG01378 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,179 |
essv23774192 | deletion | HG01432 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,051 |
essv23774193 | deletion | HG01485 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,068 |
essv23774194 | deletion | HG01495 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,329 |
essv23774195 | deletion | HG01607 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,053 |
essv23774196 | deletion | HG01766 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,435 |
essv23774197 | deletion | HG02283 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 4,207 |
essv23774198 | deletion | HG03781 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,412 |
essv23774199 | deletion | HG04171 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,431 |
essv23774200 | deletion | HG04195 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,469 |
essv23774201 | deletion | NA11893 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,664 |
essv23774202 | deletion | NA11894 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,394 |
essv23774203 | deletion | NA12045 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,512 |
essv23774204 | deletion | NA12046 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,306 |
essv23774205 | deletion | NA12399 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,513 |
essv23774206 | deletion | NA12842 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,543 |
essv23774207 | deletion | NA12873 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,054 |
essv23774208 | deletion | NA20332 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,116 |
essv23774209 | deletion | NA20516 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,702 |
essv23774210 | deletion | NA20525 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,649 |
essv23774211 | deletion | NA20534 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,666 |
essv23774212 | deletion | NA20756 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,376 |
essv23774213 | deletion | NA20809 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,667 |
essv23774214 | deletion | NA20822 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,490 |
essv23774215 | deletion | NA20885 | Sequencing | Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping | Heterozygous | 3,591 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv23774179 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774180 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774181 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774182 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774183 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774184 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774185 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774186 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774187 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774188 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774189 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774190 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774191 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774192 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774193 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774194 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774195 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774196 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774197 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774198 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774199 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774200 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774201 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774202 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774203 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774204 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774205 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774206 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774207 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774208 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774209 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774210 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774211 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774212 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774213 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774214 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774215 | Remapped | Perfect | NC_000015.10:g.(61 394545_61394751)_( 61406619_61406830) del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 61,394,751 (-206, +0) | 61,406,619 (-0, +211) |
essv23774179 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774180 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774181 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774182 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774183 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774184 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774185 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774186 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774187 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774188 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774189 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774190 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774191 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774192 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774193 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774194 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774195 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774196 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774197 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774198 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774199 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774200 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774201 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774202 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774203 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774204 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774205 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774206 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774207 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774208 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774209 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774210 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774211 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774212 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774213 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774214 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) | ||
essv23774215 | Submitted genomic | NC_000015.9:g.(616 86744_61686950)_(6 1698818_61699029)d el | GRCh37 (hg19) | NC_000015.9 | Chr15 | 61,686,950 (-206, +0) | 61,698,818 (-0, +211) |