A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621302



Internal ID21813349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35214974..35215070hg38UCSC Ensembl
chr20:33802777..33802873hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621302
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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