A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1616n100



Internal ID20153232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24367378..24455157hg38UCSC Ensembl
chr13:24941516..25029295hg19UCSC Ensembl
chr13:23839516..23927295hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3887780
hg1987780
hg1887780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041453, nsv1050215
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)dgv1616n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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