A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520599



Internal ID21844958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28396324..28396324hg38UCSC Ensembl
chr2:28619191..28619191hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040987
Supporting Variants
Samples
Known GenesFOSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520599
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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