A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542513



Internal ID20915772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21667774..21668714hg38UCSC Ensembl
chr22:22022063..22023003hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38941
hg19941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072597
Samples
Known GenesPPIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542513
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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