A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714952



Internal ID19013233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24455157..24467049hg38UCSC Ensembl
Innerchr13:25029295..25041187hg19UCSC Ensembl
Innerchr13:23927295..23939187hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3811893
hg1911893
hg1811893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035459
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)nssv3714952
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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