A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735993



Internal ID20511936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21668811..21668986hg38UCSC Ensembl
chr22:22023100..22023275hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280745
Samples
Known GenesPPIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735993
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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