nsv900070
- Organism: Homo sapiens
- Study:nstd71 (Xu et al. 2011)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:73,521
- Publication(s):Xu et al. 2011
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: 492 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 492 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 172 SVs from 16 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv900070 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 49,439,486 | 49,468,847 | 49,512,130 | 49,513,006 |
nsv900070 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 50,013,622 | 50,042,983 | 50,086,266 | 50,087,142 |
nsv900070 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 48,911,623 | 48,940,984 | 48,984,267 | 48,985,143 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv1566033 | Remapped | Perfect | NC_000013.11:g.(49 439486_49468847)_( 49512130_49513006) del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 49,439,486 | 49,468,847 | 49,512,130 | 49,513,006 |
nssv1579926 | Remapped | Perfect | NC_000013.11:g.(49 439486_49468847)_( 49512130_49513006) del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 49,439,486 | 49,468,847 | 49,512,130 | 49,513,006 |
nssv1566033 | Remapped | Perfect | NC_000013.10:g.(50 013622_50042983)_( 50086266_50087142) del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 50,013,622 | 50,042,983 | 50,086,266 | 50,087,142 |
nssv1579926 | Remapped | Perfect | NC_000013.10:g.(50 013622_50042983)_( 50086266_50087142) del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 50,013,622 | 50,042,983 | 50,086,266 | 50,087,142 |
nssv1566033 | Submitted genomic | NC_000013.9:g.(489 11623_48940984)_(4 8984267_48985143)d el | NCBI36 (hg18) | NC_000013.9 | Chr13 | 48,911,623 | 48,940,984 | 48,984,267 | 48,985,143 | ||
nssv1579926 | Submitted genomic | NC_000013.9:g.(489 11623_48940984)_(4 8984267_48985143)d el | NCBI36 (hg18) | NC_000013.9 | Chr13 | 48,911,623 | 48,940,984 | 48,984,267 | 48,985,143 |