A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561831



Internal ID16349240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:58004889..58025391hg38UCSC Ensembl
Innerchr13:58579023..58599525hg19UCSC Ensembl
Innerchr13:57477024..57497526hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3820503
hg1920503
hg1820503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv812191, nssv812190
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561831
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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