A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106550



Internal ID21271502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163971946..164017441hg38UCSC Ensembl
Innerchr3:163689734..163735229hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3845496
hg1945496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112229
Supporting Variants
Samplessample164
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106550
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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