A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095833



Internal ID21279097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26464329..26495540hg38UCSC Ensembl
Innerchr13:27038466..27069677hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3831212
hg1931212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116045
Supporting Variants
Samplessample278
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095833
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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