A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108865



Internal ID21272416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:32914347..32926409hg38UCSC Ensembl
Innerchr5:32914453..32926515hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3812063
hg1912063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111520
Supporting Variants
Samplessample177
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108865
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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