A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545092



Internal ID20918323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30745378..30750898hg38UCSC Ensembl
chr22:31141365..31146885hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg385521
hg195521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073697
Samples
Known GenesOSBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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