A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705903



Internal ID15095869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10360419..10374541hg38UCSC Ensembl
Innerchr3:10402103..10416225hg19UCSC Ensembl
Innerchr3:10377103..10391225hg18UCSC Ensembl
Innerchr3:10377103..10391225hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3814123
hg1914123
hg1814123
hg1714123
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522531
Supporting Variants
Samples
Known GenesATP2B2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705903
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer