A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675588



Internal ID15065554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15545427..15551953hg38UCSC Ensembl
Innerchr8:15402936..15409462hg19UCSC Ensembl
Innerchr8:15447307..15453833hg18UCSC Ensembl
Innerchr8:15447307..15453833hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg386527
hg196527
hg186527
hg176527
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517314
Supporting Variants
Samples
Known GenesTUSC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675588
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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