A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932270



Internal ID22236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39858781..39859257hg38UCSC Ensembl
chr3:39900272..39900748hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438281
Supporting Variants
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932270
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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