A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112834



Internal ID21296100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:148177485..148181550hg38UCSC Ensembl
Innerchr6:148498621..148502686hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg384066
hg194066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087696
Samplessample214
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112834
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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