A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619771



Internal ID21811818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:43114657..43114657hg38UCSC Ensembl
chr18:40694622..40694622hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110083
Supporting Variants
Samples
Known GenesRIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619771
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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