A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1618n100



Internal ID22787705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24454945..24467903hg38UCSC Ensembl
chr13:25029083..25042041hg19UCSC Ensembl
chr13:23927083..23940041hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3812959
hg1912959
hg1812959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043839, nsv1052526
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)dgv1618n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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