A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659992



Internal ID15049958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178593048..178597764hg38UCSC Ensembl
Innerchr3:178310836..178315552hg19UCSC Ensembl
Innerchr3:179793530..179798246hg18UCSC Ensembl
Innerchr3:179793538..179798254hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg384717
hg194717
hg184717
hg174717
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515673
Supporting Variants
Samples
Known GenesKCNMB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659992
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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