A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185272



Internal ID20752312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98044385..98044628hg38UCSC Ensembl
chr10:99804142..99804385hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438166
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185272
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.77365


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