A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692015



Internal ID15428667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133374094..133380657hg38UCSC Ensembl
Innerchr8:134386337..134392900hg19UCSC Ensembl
Innerchr8:134455519..134462082hg18UCSC Ensembl
Innerchr8:134455519..134462082hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg386564
hg196564
hg186564
hg176564
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516732
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692015
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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