A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067391



Internal ID20634431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32471338..32474851hg38UCSC Ensembl
chr20:31059141..31062654hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg383514
hg193514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518229
Supporting Variants
Samples
Known GenesC20orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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