A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108055



Internal ID21282502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85092568..85335970hg38UCSC Ensembl
Innerchr3:85141719..85385120hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38243403
hg19243402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115935
Supporting Variants
Samplessample328
Known GenesCADM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108055
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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