A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561656



Internal ID16349065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:52783965..52788560hg38UCSC Ensembl
Innerchr13:53358100..53362695hg19UCSC Ensembl
Innerchr13:52256101..52260696hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg384596
hg194596
hg184596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3147n54
Supporting Variantsnssv811691, nssv811692
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561656
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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