A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196036



Internal ID20763076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98383407..98388171hg38UCSC Ensembl
chr10:100143164..100147928hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg384765
hg194765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437465
Supporting Variants
Samples
Known GenesPYROXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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