A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714972



Internal ID19013253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:42903152..43174747hg38UCSC Ensembl
Innerchr13:43477288..43748883hg19UCSC Ensembl
Innerchr13:42375288..42646883hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38271596
hg19271596
hg18271596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052603
Supporting Variants
Samples
Known GenesDNAJC15, EPSTI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3714972
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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