A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067473



Internal ID20634513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3400439..3407830hg38UCSC Ensembl
chr20:3381086..3388477hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg387392
hg197392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530507
Supporting Variants
Samples
Known GenesC20orf194
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067473
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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