A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519058



Internal ID21843417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3321631..3321631hg38UCSC Ensembl
chr3:3363315..3363315hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040749
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519058
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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