A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056067



Internal ID21965301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43142477..43143221hg38UCSC Ensembl
chr22:43538483..43539227hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647015
Samples
Known GenesMCAT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056067
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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