A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv819909



Internal ID16113865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110914229..110915527hg38UCSC Ensembl
Innerchr13:111566576..111567874hg19UCSC Ensembl
Innerchr13:110364577..110365875hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563156
Supporting Variants
Samples
Known GenesANKRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv819909
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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