A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113458



Internal ID21296724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8701491..8707041hg38UCSC Ensembl
Innerchr8:8559001..8564551hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg385551
hg195551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086089
Samplessample218
Known GenesCLDN23
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113458
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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