A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545229



Internal ID21869584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121893681..121893681hg38UCSC Ensembl
chr3:121612528..121612528hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061593
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545229
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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