A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734921



Internal ID158587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101955047..102060748hg38UCSC Ensembl
chr3:101673891..101779592hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38105702
hg19105702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442460
Supporting Variants
Samples
Known GenesLOC152225
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734921
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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