A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083962



Internal ID21288518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:109884940..109890263hg38UCSC Ensembl
Innerchr6:110206143..110211466hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385324
hg195324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112566
Supporting Variants
Samplessample418
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083962
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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