A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561186



Internal ID16348595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18803539..18885401hg38UCSC Ensembl
Innerchr13:19377679..19459541hg19UCSC Ensembl
Innerchr13:18275679..18357541hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3881863
hg1981863
hg1881863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806023
Samples
Known GenesANKRD20A9P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561186
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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