A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3192n54



Internal ID20136616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63419953..64466355hg38UCSC Ensembl
chr13:63994086..65040487hg19UCSC Ensembl
chr13:62892087..63938488hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg381046403
hg191046402
hg181046402
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv561910, nsv561909
Samples
Known GenesLINC00395, OR7E156P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3192n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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