A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934657



Internal ID23843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60548996..60680006hg38UCSC Ensembl
chr3:60534729..60665739hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38131011
hg19131011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451393
Supporting Variants
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934657
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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