A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699572



Internal ID15436224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:79723355..79727651hg38UCSC Ensembl
Innerchr8:80635590..80639886hg19UCSC Ensembl
Innerchr8:80798145..80802441hg18UCSC Ensembl
Innerchr8:80798145..80802441hg17UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg384297
hg194297
hg184297
hg174297
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523754
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699572
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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