A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528370



Internal ID21852727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17753326..17753326hg38UCSC Ensembl
chr2:17934593..17934593hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054565
Supporting Variants
Samples
Known GenesSMC6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528370
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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