A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066317



Internal ID20633357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11333103..11334172hg38UCSC Ensembl
chr20:11313751..11314820hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg381070
hg191070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530709
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066317
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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