A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026288



Internal ID20593328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69023706..69025355hg38UCSC Ensembl
chr15:69316046..69317695hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505655
Supporting Variants
Samples
Known GenesMIR548H4, NOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00197


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