A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561896



Internal ID16349305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:62640310..62689787hg38UCSC Ensembl
Innerchr13:63214443..63263920hg19UCSC Ensembl
Innerchr13:62112444..62161921hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3849478
hg1949478
hg1849478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv812457
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561896
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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