A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104798



Internal ID22014032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50612868..50612868hg38UCSC Ensembl
chr22:51051296..51051296hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104798
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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