A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095901



Internal ID21281686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26485664..26494702hg38UCSC Ensembl
Innerchr13:27059801..27068839hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg389039
hg199039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113623
Supporting Variants
Samplessample315
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095901
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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