A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633761



Internal ID21825808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35780252..35780331hg38UCSC Ensembl
chr20:34368174..34368253hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045934
Supporting Variants
Samples
Known GenesPHF20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633761
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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