A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636186



Internal ID21828233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62231989..62232045hg38UCSC Ensembl
chr20:60807045..60807101hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047854
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636186
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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