A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14109451



Internal ID21283710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160309237..160313423hg38UCSC Ensembl
Innerchr5:159736244..159740430hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg384187
hg194187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117567
Supporting Variants
Samplessample349
Known GenesCCNJL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14109451
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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