A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066273



Internal ID20633313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11040041..11040584hg38UCSC Ensembl
chr20:11020689..11021232hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527091
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00048


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