A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108375



Internal ID21277016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4084850..4199999hg38UCSC Ensembl
Innerchr3:4126534..4241683hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38115150
hg19115150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114062
Supporting Variants
Samplessample244
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108375
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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