A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3402n54



Internal ID22771297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110913860..110915555hg38UCSC Ensembl
chr13:111566207..111567902hg19UCSC Ensembl
chr13:110364208..110365903hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381696
hg191696
hg181696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563153, nsv563151
Samples
Known GenesANKRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3402n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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