A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068140



Internal ID20635180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51832884..51834963hg38UCSC Ensembl
chr20:50449423..50451502hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg382080
hg192080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068140
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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