A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515673



Internal ID15096280
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679439, nssv664336, nssv659992
Samples
Known GenesKCNMB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515673
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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