A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622867



Internal ID21814914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50941359..50941359hg38UCSC Ensembl
chr20:49557896..49557896hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108078
Supporting Variants
Samples
Known GenesDPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622867
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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