A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523002



Internal ID21847361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217750334..217750477hg38UCSC Ensembl
chr2:218615057..218615200hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987913
Supporting Variants
Samples
Known GenesDIRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523002
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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