A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681726



Internal ID15071692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15545427..15554099hg38UCSC Ensembl
Innerchr8:15402936..15411608hg19UCSC Ensembl
Innerchr8:15447307..15455979hg18UCSC Ensembl
Innerchr8:15447307..15455979hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg388673
hg198673
hg188673
hg178673
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)nssv681726
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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