A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705736



Internal ID15442388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22979608..22980239hg38UCSC Ensembl
Innerchr8:22837121..22837752hg19UCSC Ensembl
Innerchr8:22893066..22893697hg18UCSC Ensembl
Innerchr8:22893066..22893697hg17UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38632
hg19632
hg18632
hg17632
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv529025
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705736
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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