A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094431



Internal ID21290877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:58135311..58191391hg38UCSC Ensembl
Innerchr13:58709445..58765525hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3856081
hg1956081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111002
Supporting Variants
Samplessample66
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094431
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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