A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv820163



Internal ID16114119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112765821..112767495hg38UCSC Ensembl
Innerchr13:113420135..113421809hg19UCSC Ensembl
Innerchr13:112468136..112469810hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381675
hg191675
hg181675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563234
Supporting Variants
Samples
Known GenesATP11A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv820163
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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