A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561867



Internal ID16349276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61309490..61379273hg38UCSC Ensembl
Innerchr13:61883623..61953406hg19UCSC Ensembl
Innerchr13:60781624..60851407hg18UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3869784
hg1969784
hg1869784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176049
Samples1780862312_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561867
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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