A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190008



Internal ID21328854
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3950274
Supporting Variants
SamplesHG002
Known GenesTSPO
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190008
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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