A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937540



Internal ID25745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107968330..108404715hg38UCSC Ensembl
chr3:107687177..108123562hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38436386
hg19436386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440090
Supporting Variants
Samples
Known GenesCD47, HHLA2, IFT57, MYH15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937540
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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