esv3619665
- Organism: Homo sapiens
- Study:estd214 (1000 Genomes Consortium Phase 3)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:35
- Validation:Not tested
- Clinical Assertions: No
- Region Size:113,334
- Publication(s):1000 Genomes Project Consortium et al. 2015
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: 2444 SVs from 94 studies. See in: genome view
Overlapping variant regions from other studies: 2448 SVs from 94 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3619665 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| esv3619665 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Zygosity | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| essv13404368 | deletion | SAMN00004672 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,782 |
| essv13404369 | deletion | SAMN01036843 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,809 |
| essv13404370 | deletion | SAMN00006516 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,414 |
| essv13404371 | deletion | SAMN00006529 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,283 |
| essv13404372 | deletion | SAMN00006541 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,595 |
| essv13404373 | deletion | SAMN00009123 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,733 |
| essv13404374 | deletion | SAMN00009126 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,768 |
| essv13404375 | deletion | SAMN00009151 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,226 |
| essv13404376 | deletion | SAMN00009254 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,508 |
| essv13404377 | deletion | SAMN00014350 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,736 |
| essv13404378 | deletion | SAMN00249814 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,794 |
| essv13404379 | deletion | SAMN00249920 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,784 |
| essv13404380 | deletion | SAMN00249921 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,838 |
| essv13404381 | deletion | SAMN00255150 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,737 |
| essv13404382 | deletion | SAMN00249927 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,787 |
| essv13404383 | deletion | SAMN01761374 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,800 |
| essv13404384 | deletion | SAMN01090780 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,063 |
| essv13404385 | deletion | SAMN01761266 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,677 |
| essv13404386 | deletion | SAMN01761455 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,258 |
| essv13404387 | deletion | SAMN01761586 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,954 |
| essv13404388 | deletion | SAMN00000423 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,679 |
| essv13404389 | deletion | SAMN00000442 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,272 |
| essv13404390 | deletion | SAMN00000450 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,860 |
| essv13404391 | deletion | SAMN00000467 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,654 |
| essv13404392 | deletion | SAMN00000487 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,549 |
| essv13404393 | deletion | SAMN00001645 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,668 |
| essv13404394 | deletion | SAMN00001653 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,616 |
| essv13404395 | deletion | SAMN00001031 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,826 |
| essv13404396 | deletion | SAMN00001038 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,794 |
| essv13404397 | deletion | SAMN00000527 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,928 |
| essv13404398 | deletion | SAMN00001339 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,222 |
| essv13404399 | deletion | SAMN00001155 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,979 |
| essv13404400 | deletion | SAMN00004488 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,855 |
| essv13404401 | deletion | SAMN00007953 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,763 |
| essv13404402 | deletion | SAMN00007976 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,833 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv13404368 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404369 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404370 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404371 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404372 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404373 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404374 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404375 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404376 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404377 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404378 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404379 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404380 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404381 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404382 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404383 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404384 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404385 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404386 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404387 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404388 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404389 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404390 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404391 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404392 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404393 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404394 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404395 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404396 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404397 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404398 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404399 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404400 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404401 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404402 | Remapped | Perfect | NC_000009.12:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |
| essv13404368 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404369 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404370 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404371 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404372 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404373 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404374 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404375 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404376 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404377 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404378 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404379 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404380 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404381 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404382 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404383 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404384 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404385 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404386 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404387 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404388 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404389 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404390 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404391 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404392 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404393 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404394 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404395 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404396 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404397 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404398 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404399 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404400 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404401 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) | ||
| essv13404402 | Submitted genomic | NC_000009.11:g.(12 007134_12008634)_( 12120967_12122467) del | GRCh37 (hg19) | NC_000009.11 | Chr9 | 12,008,134 (-1000, +500) | 12,121,467 (-500, +1000) |