A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932271



Internal ID22237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39876500..39886000hg38UCSC Ensembl
chr3:39917991..39927491hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg389501
hg199501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443264
Supporting Variants
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932271
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001874


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