A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561567



Internal ID16002290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:43012948..43033007hg38UCSC Ensembl
Innerchr13:43587084..43607143hg19UCSC Ensembl
Innerchr13:42485084..42505143hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3820060
hg1920060
hg1820060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175932
SamplesHGDP01100
Known GenesDNAJC15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561567
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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