nsv5905
- Organism: Homo sapiens
- Study:nstd2 (Kidd et al. 2008)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Yes
- Clinical Assertions: No
- Region Size:76,373
- Publication(s):Kidd et al. 2008
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 319 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 319 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 12 SVs from 8 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5905 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 112,805,370 | 112,881,742 |
nsv5905 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 112,445,425 | 112,521,797 |
nsv5905 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000007.11 | Chr7 | 112,039,376 | 112,115,748 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv6162 | Remapped | Perfect | NC_000007.14:g.(11 2805370_?)_(?_1128 50956)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 112,805,370 | 112,850,956 |
nssv10575 | Remapped | Perfect | NC_000007.14:g.(11 2844175_?)_(?_1128 81742)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 112,844,175 | 112,881,742 |
nssv6162 | Remapped | Perfect | NC_000007.13:g.(11 2445425_?)_(?_1124 91011)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 112,445,425 | 112,491,011 |
nssv10575 | Remapped | Perfect | NC_000007.13:g.(11 2484230_?)_(?_1125 21797)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 112,484,230 | 112,521,797 |
nssv6162 | Submitted genomic | NC_000007.11:g.(11 2039376_?)_(?_1120 84962)del6163 | NCBI35 (hg17) | NC_000007.11 | Chr7 | 112,039,376 | 112,084,962 | ||
nssv10575 | Submitted genomic | NC_000007.11:g.(11 2078181_?)_(?_1121 15748)del7861 | NCBI35 (hg17) | NC_000007.11 | Chr7 | 112,078,181 | 112,115,748 |