A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882681



Internal ID22657658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41438936..41441285hg38UCSC Ensembl
chr22:41834940..41837289hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg382350
hg192350
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483540
Samples
Known GenesTOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882681
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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