A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627937



Internal ID21819984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36976275..36976754hg38UCSC Ensembl
chr20:35604678..35605157hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044331
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627937
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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