A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628072



Internal ID21820119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52900874..52900874hg38UCSC Ensembl
chr20:51517413..51517413hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104879
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628072
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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