A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950274



Internal ID21370343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43153014..43153014hg38UCSC Ensembl
chr22:43549020..43549020hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190008
SamplesHG002
Known GenesTSPO
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950274
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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