A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482902



Internal ID22540808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35364856..35388514hg38UCSC Ensembl
chr22:35760849..35784507hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3823659
hg1923659
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875998
Supporting Variants
Samples
Known GenesHMOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482902
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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