A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116958



Internal ID21300224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140065085..140069124hg38UCSC Ensembl
Innerchr6:140386222..140390261hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg384040
hg194040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083102, nssv14084421
Samplessample87, sample362
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116958
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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