A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050816



Internal ID21960049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39101609..39101672hg38UCSC Ensembl
chr22:39497614..39497677hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641327
Samples
Known GenesAPOBEC3H
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050816
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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