A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050147



Internal ID21959380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31002043..31003626hg38UCSC Ensembl
chr22:31398029..31399612hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381584
hg191584
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050147
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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