A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934240



Internal ID23559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75137681..75140608hg38UCSC Ensembl
chr3:75186832..75189759hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg382928
hg192928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934240
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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