nsv441897
- Organism: Homo sapiens
- Study:nstd22 (McCarroll et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:57,352
- Publication(s):McCarroll et al. 2008
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: 356 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 356 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 22 SVs from 7 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 |
---|---|---|---|---|---|---|---|---|---|
nsv441897 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 88,102,936 | 88,160,287 |
nsv441897 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 89,024,088 | 89,081,439 |
nsv441897 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000004.9 | Chr4 | 89,381,267 | 89,438,618 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1657606 | Remapped | Perfect | NC_000004.12:g.(?_ 88102936)_(8816028 7_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 88,102,936 | 88,160,287 |
nssv1657607 | Remapped | Perfect | NC_000004.12:g.(?_ 88102936)_(8816028 7_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 88,102,936 | 88,160,287 |
nssv1657606 | Remapped | Perfect | NC_000004.11:g.(?_ 89024088)_(8908143 9_?)dup | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 89,024,088 | 89,081,439 |
nssv1657607 | Remapped | Perfect | NC_000004.11:g.(?_ 89024088)_(8908143 9_?)dup | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 89,024,088 | 89,081,439 |
nssv1657606 | Submitted genomic | NC_000004.9:g.(?_8 9381267)_(89438618 _?)dup | NCBI35 (hg17) | NC_000004.9 | Chr4 | 89,381,267 | 89,438,618 | ||
nssv1657607 | Submitted genomic | NC_000004.9:g.(?_8 9381267)_(89438618 _?)dup | NCBI35 (hg17) | NC_000004.9 | Chr4 | 89,381,267 | 89,438,618 |