A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553792



Internal ID21878147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133049003..133049003hg38UCSC Ensembl
chr3:132767847..132767847hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067787
Supporting Variants
Samples
Known GenesTMEM108
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553792
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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