A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539233



Internal ID20912537
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 StatusM
Merged Variants
Supporting Variantsnssv18073417
Samples
Known GenesLOC284889, MIF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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