A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693651



Internal ID15430303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95199592..95223223hg38UCSC Ensembl
Innerchr8:96211820..96235451hg19UCSC Ensembl
Innerchr8:96280996..96304627hg18UCSC Ensembl
Innerchr8:96280996..96304627hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3823632
hg1923632
hg1823632
hg1723632
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516035
Supporting Variants
Samples
Known GenesC8orf69
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693651
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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