A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520105



Internal ID20893466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46167785..46170930hg38UCSC Ensembl
chr18:43747751..43750896hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg383146
hg193146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520105
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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