A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647601



Internal ID21839648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35389395..35389395hg38UCSC Ensembl
chr22:35785388..35785388hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109527
Supporting Variants
Samples
Known GenesHMOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647601
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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