A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014953



Internal ID18757488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179260056..179288845hg38UCSC Ensembl
Innerchr3:178977844..179006633hg19UCSC Ensembl
Innerchr3:180460538..180489327hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3828790
hg1928790
hg1828790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5000n100
Supporting Variantsnssv3614993
Samples
Known GenesKCNMB3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014953
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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