A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106099



Internal ID22015332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47732315..47732315hg38UCSC Ensembl
chr22:48128064..48128064hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639179
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106099
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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