A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083977



Internal ID21288744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:120660896..120687561hg38UCSC Ensembl
Innerchr6:120982042..121008707hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3826666
hg1926666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114202
Supporting Variants
Samplessample420
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083977
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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