A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561586



Internal ID16348995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:47248841..47268545hg38UCSC Ensembl
Innerchr13:47822976..47842680hg19UCSC Ensembl
Innerchr13:46720977..46740681hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3819705
hg1919705
hg1819705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175936
Samples1780854257_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561586
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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