A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110730



Internal ID22019963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32333352..32333352hg38UCSC Ensembl
chr22:32729339..32729339hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643511
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110730
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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