A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105627



Internal ID22014860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50193929..50193929hg38UCSC Ensembl
chr22:50632358..50632358hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640279
Samples
Known GenesTRABD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105627
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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