A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17405495



Internal ID22463365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:22166095..22398164hg38UCSC Ensembl
chr22:22520488..22752499hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38232070
hg19232012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959043
Supporting Variants
Samples
Known GenesBMS1P20, VPREB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17405495
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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