A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218297



Internal ID20785337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22166201..22172400hg38UCSC Ensembl
chr6:22166430..22172629hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396008
Supporting Variants
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218297
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0012


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