A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074998



Internal ID20642038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:46713315..46729835hg38UCSC Ensembl
chr22:47109212..47125732hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3816521
hg1916521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554048
Supporting Variants
Samples
Known GenesCERK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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