A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039478



Internal ID20606518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24447399..24448057hg38UCSC Ensembl
chr18:22027363..22028021hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534138
Supporting Variants
Samples
Known GenesIMPACT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039478
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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