A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199735



Internal ID20766775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114509701..114512500hg38UCSC Ensembl
chr1:115052322..115055121hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324317
Supporting Variants
Samples
Known GenesTRIM33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199735
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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