A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv811667



Internal ID16105623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:50711947..50732194hg38UCSC Ensembl
Innerchr13:51286083..51306330hg19UCSC Ensembl
Innerchr13:50184084..50204331hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3820248
hg1920248
hg1820248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561643
Supporting Variants
Samples
Known GenesDLEU7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv811667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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