A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699322



Internal ID15435974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:103313106..103313995hg38UCSC Ensembl
Innerchr8:104325334..104326223hg19UCSC Ensembl
Innerchr8:104394510..104395399hg18UCSC Ensembl
Innerchr8:104394510..104395399hg17UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38890
hg19890
hg18890
hg17890
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523544
Supporting Variants
Samples
Known GenesFZD6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699322
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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