A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087616



Internal ID21273684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121833399..121838283hg38UCSC Ensembl
Innerchr6:122154545..122159429hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384885
hg194885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111274
Supporting Variants
Samplessample194
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087616
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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