A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561587



Internal ID16348996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:47345476..47404117hg38UCSC Ensembl
Innerchr13:47919611..47978252hg19UCSC Ensembl
Innerchr13:46817612..46876253hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3858642
hg1958642
hg1858642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175937
SamplesHGDP00682
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561587
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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