A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875998



Internal ID22650958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35364856..35388514hg38UCSC Ensembl
chr22:35760849..35784507hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3823659
hg1923659
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482902
Samples
Known GenesHMOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875998
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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