A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083779



Internal ID21292060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140065085..140070644hg38UCSC Ensembl
Innerchr6:140386222..140391781hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg385560
hg195560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111817
Supporting Variants
Samplessample82
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083779
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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