A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934326



Internal ID23615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78468141..78468876hg38UCSC Ensembl
chr3:78517291..78518026hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934326
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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