A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103500



Internal ID21277857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:133078234..133080538hg38UCSC Ensembl
Innerchr3:132797078..132799382hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382305
hg192305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116080
Supporting Variants
Samplessample26
Known GenesTMEM108
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103500
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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