A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561713



Internal ID16349122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55898868..56035002hg38UCSC Ensembl
Innerchr13:56473002..56609136hg19UCSC Ensembl
Innerchr13:55371003..55507137hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38136135
hg19136135
hg18136135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv811799
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561713
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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