A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522237



Internal ID20895598
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 StatusM
Merged Variants
Supporting Variantsnssv18187266
Samples
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522237
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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