A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116646



Internal ID21299912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:80589826..80932804hg38UCSC Ensembl
Innerchr4:81510980..81853958hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38342979
hg19342979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107108
Samplessample1
Known GenesC4orf22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116646
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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