A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739671



Internal ID18691266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:33386293..33565948hg38UCSC Ensembl
Innerchr3:33427785..33607440hg19UCSC Ensembl
Innerchr3:33402789..33582444hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38179656
hg19179656
hg18179656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001132
Supporting Variants
Samples
Known GenesCLASP2, FBXL2, UBP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3739671
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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