A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940982



Internal ID28025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139027574..139067574hg38UCSC Ensembl
chr3:138746416..138786416hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3840001
hg1940001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453712
Supporting Variants
Samples
Known GenesPRR23C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940982
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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