A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052526



Internal ID19141745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24454945..24467049hg38UCSC Ensembl
Innerchr13:25029083..25041187hg19UCSC Ensembl
Innerchr13:23927083..23939187hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3812105
hg1912105
hg1812105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1618n100
Supporting Variantsnssv3523184
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)nsv1052526
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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