A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525896



Internal ID21850254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223408334..223408334hg38UCSC Ensembl
chr2:224273052..224273052hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054216
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525896
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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