A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287569



Internal ID20496787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44305984..44306045hg38UCSC Ensembl
chr20:42934624..42934685hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744464
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287569
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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