A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877808



Internal ID22652773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41432609..41435172hg38UCSC Ensembl
chr22:41828613..41831176hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg382564
hg192564
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483538
Samples
Known GenesTOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877808
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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