A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628221



Internal ID21820268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1668125..1668176hg38UCSC Ensembl
chr20:1648771..1648822hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050463
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628221
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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