A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626796



Internal ID21818843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34245185..34245278hg38UCSC Ensembl
chr20:32832991..32833084hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044661
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626796
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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