A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146507



Internal ID345712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:22031472..22245534hg38UCSC Ensembl
chr22:22385870..22599946hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38214063
hg19214077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727841
Samples
Known GenesVPREB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146507
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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