A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523162



Internal ID18474757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24367378..24438885hg38UCSC Ensembl
Innerchr13:24941516..25013023hg19UCSC Ensembl
Innerchr13:23839516..23911023hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3871508
hg1971508
hg1871508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041453
Supporting Variants
Samples
Known GenesPARP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523162
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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