A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934226



Internal ID23550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72122589..72122731hg38UCSC Ensembl
chr3:72171740..72171882hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439827
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934226
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005776


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