A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542951



Internal ID21867306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69055634..69055634hg38UCSC Ensembl
chr3:69104785..69104785hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg382022
hg192022
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6077044
Supporting Variants
Samples
Known GenesUBA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542951
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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