A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619592



Internal ID21811639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40259614..40259718hg38UCSC Ensembl
chr20:38888254..38888358hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046093
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619592
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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