A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691279



Internal ID15081245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13682049..13682977hg38UCSC Ensembl
Innerchr8:13539558..13540486hg19UCSC Ensembl
Innerchr8:13583929..13584857hg18UCSC Ensembl
Innerchr8:13583929..13584857hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38929
hg19929
hg18929
hg17929
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517019
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691279
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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