A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546191



Internal ID21870546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:124898654..124899875hg38UCSC Ensembl
chr3:124617501..124618722hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg381222
hg191222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546191
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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