A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3226n54



Internal ID22771121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68666591..68698681hg38UCSC Ensembl
chr13:69240723..69272813hg19UCSC Ensembl
chr13:68138724..68170814hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3832091
hg1932091
hg1832091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562159, nsv562155, nsv562162, nsv562161, nsv562157, nsv562156, nsv562160
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3226n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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