A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561708



Internal ID16349117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55563288..55843136hg38UCSC Ensembl
Innerchr13:56137423..56417270hg19UCSC Ensembl
Innerchr13:55035424..55315271hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38279849
hg19279848
hg18279848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv811797
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561708
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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