A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067359



Internal ID20634399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31521801..31523500hg38UCSC Ensembl
chr20:30109604..30111303hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531691
Supporting Variants
Samples
Known GenesHM13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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