A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939701



Internal ID27188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141519509..141526829hg38UCSC Ensembl
chr3:141238351..141245671hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg387321
hg197321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440553
Supporting Variants
Samples
Known GenesRASA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939701
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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