A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv810401



Internal ID16104357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:49939063..49940038hg38UCSC Ensembl
Innerchr13:50513199..50514174hg19UCSC Ensembl
Innerchr13:49411200..49412175hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38976
hg19976
hg18976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561628
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv810401
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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