A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3302n54



Internal ID22771197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88853238..88912396hg38UCSC Ensembl
chr13:89505492..89564650hg19UCSC Ensembl
chr13:88303493..88362651hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3859159
hg1959159
hg1859159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562638, nsv562637
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3302n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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