A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051907



Internal ID21961140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44262286..44263405hg38UCSC Ensembl
chr22:44658166..44659285hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381120
hg191120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645122
Samples
Known GenesKIAA1644
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051907
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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