A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045262



Internal ID21954530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21691386..21691509hg38UCSC Ensembl
chr22:22045675..22045798hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647381
Samples
Known GenesPPIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045262
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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