A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3286n54



Internal ID22771181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83360626..83456379hg38UCSC Ensembl
chr13:83934761..84030514hg19UCSC Ensembl
chr13:82832762..82928515hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3895754
hg1995754
hg1895754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562514, nsv562512, nsv562513
SamplesNINDS_183
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3286n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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