A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105385



Internal ID22014618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35533643..35533643hg38UCSC Ensembl
chr22:35929690..35929690hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105385
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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