A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17530914



Internal ID21855270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216484060..216490548hg38UCSC Ensembl
chr2:217348783..217355271hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg386489
hg196489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987540
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17530914
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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