A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656904



Internal ID15393556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:1962492..1963227hg38UCSC Ensembl
Innerchr8:1910658..1911393hg19UCSC Ensembl
Innerchr8:1898065..1898800hg18UCSC Ensembl
Innerchr8:1898065..1898800hg17UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38736
hg19736
hg18736
hg17736
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517213
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656904
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