A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518899



Internal ID20892260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24184500..24191199hg38UCSC Ensembl
chr18:21764464..21771163hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040398
Samples
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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