A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732837



Internal ID19031118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65203548..65222043hg38UCSC Ensembl
Innerchr3:65189223..65207718hg19UCSC Ensembl
Innerchr3:65164263..65182758hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3818496
hg1918496
hg1818496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003976
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3732837
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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