A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086334



Internal ID21268227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140065085..140071152hg38UCSC Ensembl
Innerchr6:140386222..140392289hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg386068
hg196068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113405
Supporting Variants
Samplessample122
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086334
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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