A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3403n54



Internal ID22771298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110914065..110915527hg38UCSC Ensembl
chr13:111566412..111567874hg19UCSC Ensembl
chr13:110364413..110365875hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381463
hg191463
hg181463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563156, nsv563152
Samples
Known GenesANKRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3403n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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