A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026045



Internal ID20593085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60649819..60650407hg38UCSC Ensembl
chr15:60942018..60942606hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498781
Supporting Variants
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026045
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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