A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705092



Internal ID15441744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2738450..2739803hg38UCSC Ensembl
Innerchr8:2595978..2597331hg19UCSC Ensembl
Innerchr8:2583385..2584738hg18UCSC Ensembl
Innerchr8:2583385..2584738hg17UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg381354
hg191354
hg181354
hg171354
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515930
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705092
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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