A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073417



Internal ID20640457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23891511..23894561hg38UCSC Ensembl
chr22:24233698..24236748hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg383051
hg193051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539233
Supporting Variants
Samples
Known GenesLOC284889, MIF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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