A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108100



Internal ID21283091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:168112271..168119942hg38UCSC Ensembl
Innerchr3:167830059..167837730hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg387672
hg197672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115330
Supporting Variants
Samplessample339
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108100
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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