A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163519



Internal ID20730559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115532167..115532852hg38UCSC Ensembl
chr8:116544394..116545079hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425311
Supporting Variants
Samples
Known GenesTRPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163519
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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