A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520882



Internal ID21845241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:233403327..233403442hg38UCSC Ensembl
chr2:234311973..234312088hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5988011
Supporting Variants
Samples
Known GenesDGKD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520882
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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