A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107861



Internal ID21279898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:157635761..157641117hg38UCSC Ensembl
Innerchr3:157353550..157358906hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg385357
hg195357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118323
Supporting Variants
Samplessample290
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107861
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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