A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139437



Internal ID338622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111573692..111573752hg38UCSC Ensembl
chr3:111292539..111292599hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937953
Samples
Known GenesCD96
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139437
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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