A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067341



Internal ID20634381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3111294..3123201hg38UCSC Ensembl
chr20:3091940..3103847hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3811908
hg1911908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535438
Supporting Variants
Samples
Known GenesUBOX5, UBOX5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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