A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561660



Internal ID16349069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:52784795..52788904hg38UCSC Ensembl
Innerchr13:53358930..53363039hg19UCSC Ensembl
Innerchr13:52256931..52261040hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg384110
hg194110
hg184110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3147n54
Supporting Variantsnssv811697
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561660
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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