A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629417



Internal ID21821464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53935679..53935679hg38UCSC Ensembl
chr20:52552218..52552218hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105688
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629417
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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