A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697417



Internal ID15434069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94586370..94596139hg38UCSC Ensembl
Innerchr8:95598598..95608367hg19UCSC Ensembl
Innerchr8:95667774..95677543hg18UCSC Ensembl
Innerchr8:95667774..95677543hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg389770
hg199770
hg189770
hg179770
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520435
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697417
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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