A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083556



Internal ID21282669
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 StatusS
Merged Variantsnsv3112867
Supporting Variants
Samplessample33
Known GenesDCBLD1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083556
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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