A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620369



Internal ID21812416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2475228..2475228hg38UCSC Ensembl
chr20:2455874..2455874hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108633
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620369
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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