A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187266



Internal ID20754306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24385028..24393236hg38UCSC Ensembl
chr18:21964992..21973200hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg388209
hg198209
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522237
Supporting Variants
Samples
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187266
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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