A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645094



Internal ID21837141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42634251..42634308hg38UCSC Ensembl
chr22:43030257..43030314hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042169
Supporting Variants
Samples
Known GenesCYB5R3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645094
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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