A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535359



Internal ID21859714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145891294..145891294hg38UCSC Ensembl
chr2:146648862..146648862hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041451
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535359
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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