A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694481



Internal ID15431133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10944592..10978962hg38UCSC Ensembl
Innerchr8:10802102..10836472hg19UCSC Ensembl
Innerchr8:10839512..10873882hg18UCSC Ensembl
Innerchr8:10839512..10873882hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3834371
hg1934371
hg1834371
hg1734371
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521721
Supporting Variants
Samples
Known GenesXKR6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694481
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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