A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039473



Internal ID20606513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24365219..24392276hg38UCSC Ensembl
chr18:21945183..21972240hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3827058
hg1927058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523613
Supporting Variants
Samples
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039473
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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