A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112867



Internal ID21296133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:117480130..117485303hg38UCSC Ensembl
Innerchr6:117801293..117806466hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg385174
hg195174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083556
Samplessample33
Known GenesDCBLD1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112867
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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