A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669676



Internal ID15059642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13757626..13792292hg38UCSC Ensembl
Innerchr8:13615135..13649801hg19UCSC Ensembl
Innerchr8:13659506..13694172hg18UCSC Ensembl
Innerchr8:13659506..13694172hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3834667
hg1934667
hg1834667
hg1734667
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)nssv669676
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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