nsv4373337
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:44
- Validation:Not tested
- Clinical Assertions: No
- Region Size:55,058
- Publication(s):Zarrei et al. 2019
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: 528 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 589 SVs from 77 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4373337 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nsv4373337 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv15611624 | copy number loss | 1-0650-003 | SNP array | Genotyping | 18 |
nssv15611852 | copy number loss | 1-0657-003 | SNP array | Genotyping | 21 |
nssv15614125 | copy number loss | 1-0731-004 | SNP array | Genotyping | 16 |
nssv15615472 | copy number gain | 1-0775-003 | SNP array | Genotyping | 18 |
nssv15615723 | copy number gain | 1-0777-003 | SNP array | Genotyping | 26 |
nssv15620334 | copy number loss | 1-0962-003 | SNP array | Genotyping | 27 |
nssv15621971 | copy number loss | 1-1001-003 | SNP array | Genotyping | 29 |
nssv15623292 | copy number loss | 1-0244-001 | SNP array | Genotyping | 16 |
nssv15623911 | copy number loss | 1-0271-004 | SNP array | Genotyping | 29 |
nssv15624059 | copy number loss | 1-0290-003 | SNP array | Genotyping | 25 |
nssv15624188 | copy number gain | 1-0262-002 | SNP array | Genotyping | 28 |
nssv15626483 | copy number loss | 1-0441-001 | SNP array | Genotyping | 19 |
nssv15626524 | copy number loss | 1-0441-003 | SNP array | Genotyping | 20 |
nssv15632478 | copy number loss | 10-0007-002 | SNP array | Genotyping | 26 |
nssv15634492 | copy number loss | 11-0046-003 | SNP array | Genotyping | 15 |
nssv15634545 | copy number gain | 12-4261-003 | SNP array | Genotyping | 28 |
nssv15634940 | copy number gain | 12-4425-002 | SNP array | Genotyping | 26 |
nssv15636911 | copy number loss | 14-0017-003 | SNP array | Genotyping | 18 |
nssv15638315 | copy number gain | 14-0062-002 | SNP array | Genotyping | 16 |
nssv15646953 | copy number gain | 2-1094-005 | SNP array | Genotyping | 17 |
nssv15648324 | copy number gain | 2-1276-003 | SNP array | Genotyping | 21 |
nssv15651456 | copy number gain | 2-1437-001 | SNP array | Genotyping | 28 |
nssv15653898 | copy number gain | 2-1605-004 | SNP array | Genotyping | 24 |
nssv15654147 | copy number loss | 2-1584-003 | SNP array | Genotyping | 20 |
nssv15655783 | copy number loss | 2-1722-003 | SNP array | Genotyping | 15 |
nssv15656223 | copy number loss | 3-0709-000 | SNP array | Genotyping | 19 |
nssv15657349 | copy number loss | 3-0481-000 | SNP array | Genotyping | 17 |
nssv15659911 | copy number loss | 5-0001-002 | SNP array | Genotyping | 23 |
nssv15662097 | copy number loss | 5-0084-004 | SNP array | Genotyping | 19 |
nssv15663994 | copy number gain | 5-0144-001 | SNP array | Genotyping | 23 |
nssv15667227 | copy number loss | 7-0152-003 | SNP array | Genotyping | 22 |
nssv15669329 | copy number loss | 7-0220-003 | SNP array | Genotyping | 33 |
nssv15669700 | copy number loss | 7-0237-003 | SNP array | Genotyping | 21 |
nssv15671316 | copy number loss | 7-0280-005 | SNP array | Genotyping | 18 |
nssv15674211 | copy number loss | 9-0023-001 | SNP array | Genotyping | 19 |
nssv15688084 | copy number gain | 208024 | SNP array | Genotyping | 13 |
nssv15690286 | copy number loss | OCD141-0625-7921-1 | SNP array | Genotyping | 29 |
nssv15697736 | copy number loss | 176792 | SNP array | Genotyping | 13 |
nssv15699099 | copy number loss | 196902 | SNP array | Genotyping | 15 |
nssv15700147 | copy number gain | 183791 | SNP array | Genotyping | 23 |
nssv15700191 | copy number loss | 197234 | SNP array | Genotyping | 10 |
nssv15700638 | copy number loss | 196405 | SNP array | Genotyping | 22 |
nssv15701064 | copy number loss | 185747 | SNP array | Genotyping | 19 |
nssv15702021 | copy number loss | 199158 | SNP array | Genotyping | 16 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15611624 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15611852 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15614125 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15615472 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15615723 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15620334 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15621971 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15623292 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15623911 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15624059 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15624188 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15626483 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15626524 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15632478 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15634492 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15634545 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15634940 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15636911 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15638315 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15646953 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15648324 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15651456 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15653898 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15654147 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15655783 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15656223 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15657349 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15659911 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15662097 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15663994 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15667227 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15669329 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15669700 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15671316 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15674211 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15688084 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15690286 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15697736 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15699099 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15700147 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15700191 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15700638 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15701064 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15702021 | Remapped | Pass | NC_000002.12:g.(?_ 97490656)_(9754571 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,490,656 | 97,545,713 |
nssv15611624 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15611852 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15614125 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15615472 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15615723 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15620334 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15621971 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15623292 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15623911 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15624059 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15624188 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15626483 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15626524 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15632478 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15634492 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15634545 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15634940 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15636911 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15638315 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15646953 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15648324 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15651456 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15653898 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15654147 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15655783 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15656223 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15657349 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15659911 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15662097 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15663994 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15667227 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15669329 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15669700 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15671316 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15674211 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15688084 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15690286 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15697736 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15699099 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15700147 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15700191 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15700638 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15701064 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 | ||
nssv15702021 | Submitted genomic | NC_000002.11:g.(?_ 98063359)_(9816217 6_?)del | GRCh37 (hg19) | NC_000002.11 | Chr2 | 98,063,359 | 98,162,176 |