A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043839



Internal ID19133058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24455238..24467903hg38UCSC Ensembl
Innerchr13:25029376..25042041hg19UCSC Ensembl
Innerchr13:23927376..23940041hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3812666
hg1912666
hg1812666
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1618n100
Supporting Variantsnssv3523185
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)nsv1043839
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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