A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066229



Internal ID20633269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10310046..10310674hg38UCSC Ensembl
chr20:10290694..10291322hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522802
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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