A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108326



Internal ID21276374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163971946..164020009hg38UCSC Ensembl
Innerchr3:163689734..163737797hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3848064
hg1948064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112337
Supporting Variants
Samplessample235
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108326
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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