A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687189



Internal ID15423841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46033291..46828229hg38UCSC Ensembl
Innerchr8:46944913..47739851hg19UCSC Ensembl
Innerchr8:47064078..47859016hg18UCSC Ensembl
Innerchr8:47064078..47859016hg17UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38794939
hg19794939
hg18794939
hg17794939
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687189
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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