A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623685



Internal ID21815732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54219880..54239816hg38UCSC Ensembl
chr19:54723749..54743692hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3819937
hg1919944
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048932
Supporting Variants
Samples
Known GenesLILRA6, LILRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623685
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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