A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885547



Internal ID22660531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43382176..43389406hg38UCSC Ensembl
chr22:43778182..43785412hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg387231
hg197231
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885547
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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