A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154899



Internal ID22085404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:52986321..53014734hg38UCSC Ensembl
Outerchr13:52979915..53020753hg38UCSC Ensembl
Innerchr13:53560456..53588869hg19UCSC Ensembl
Outerchr13:53554050..53594888hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3840839
hg1940839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008106
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154899
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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