A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3276n54



Internal ID22771171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:81930550..82053453hg38UCSC Ensembl
chr13:82504685..82627588hg19UCSC Ensembl
chr13:81402686..81525589hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38122904
hg19122904
hg18122904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562452, nsv562451
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3276n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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