A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941146



Internal ID21361215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39698775..39698775hg38UCSC Ensembl
chr22:40094780..40094780hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189984
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941146
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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