A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870533



Internal ID22645469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43090083..43102545hg38UCSC Ensembl
chr22:43486089..43498551hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3812463
hg1912463
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483624
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870533
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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