A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097316



Internal ID21292301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114639414..114684125hg38UCSC Ensembl
Innerchr5:113975111..114019822hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3844712
hg1944712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112900
Supporting Variants
Samplessample87
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097316
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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