A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068840



Internal ID20635880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38441532..38447323hg38UCSC Ensembl
chr20:37070175..37075966hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg385792
hg195792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515858
Supporting Variants
Samples
Known GenesSNHG11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068840
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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