A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089234



Internal ID21279917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:129445699..129447582hg38UCSC Ensembl
Innerchr6:129766844..129768727hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg381884
hg191884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110859
Supporting Variants
Samplessample290
Known GenesLAMA2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089234
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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