A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934775



Internal ID23918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67307492..67588204hg38UCSC Ensembl
chr3:67357916..67638628hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38280713
hg19280713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440311
Supporting Variants
Samples
Known GenesSUCLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934775
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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