A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010137



Internal ID18752668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179245109..179332999hg38UCSC Ensembl
Innerchr3:178962897..179050787hg19UCSC Ensembl
Innerchr3:180445591..180533481hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3887891
hg1987891
hg1887891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614992
Samples
Known GenesKCNMB3, ZNF639
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010137
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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