A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108541



Internal ID21284041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:31533273..31534450hg38UCSC Ensembl
Innerchr3:31574765..31575942hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg381178
hg191178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112299
Supporting Variants
Samplessample357
Known GenesSTT3B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108541
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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