A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657435



Internal ID15394087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3750416..3752893hg38UCSC Ensembl
Innerchr10:3792608..3795085hg19UCSC Ensembl
Innerchr10:3782608..3785085hg18UCSC Ensembl
Innerchr10:3782608..3785085hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg382478
hg192478
hg182478
hg172478
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517787
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657435
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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