A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3404n54



Internal ID22771299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110914065..110915799hg38UCSC Ensembl
chr13:111566412..111568146hg19UCSC Ensembl
chr13:110364413..110366147hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381735
hg191735
hg181735
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563155, nsv563154, nsv563157
Samples
Known GenesANKRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3404n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss3
Observed Complex0
Frequencyn/a


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