A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073698



Internal ID20640738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30780524..30781377hg38UCSC Ensembl
chr22:31176511..31177364hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554708
Supporting Variants
Samples
Known GenesOSBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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