A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108577



Internal ID21284566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4199999..4236672hg38UCSC Ensembl
Innerchr3:4241683..4278356hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3836674
hg1936674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114991
Supporting Variants
Samplessample362
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108577
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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