A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107854



Internal ID22017088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36074097..36074097hg38UCSC Ensembl
chr22:36470145..36470145hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107854
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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