A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069115



Internal ID20636155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58386022..58387687hg38UCSC Ensembl
chr20:56961078..56962743hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg381666
hg191666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551257
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069115
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00065


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