A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200258



Internal ID20767298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54232601..54238000hg38UCSC Ensembl
chr19:54736477..54741876hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526084
Supporting Variants
Samples
Known GenesLILRA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200258
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.22491


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