A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963876



Internal ID22738812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35356512..35388774hg38UCSC Ensembl
chr22:35752505..35784767hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3832263
hg1932263
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393449
Samples
Known GenesHMOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963876
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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