A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198057



Internal ID20765097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11145013..11151896hg38UCSC Ensembl
chr19:11255689..11262572hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg386884
hg196884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519798
Supporting Variants
Samples
Known GenesSPC24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198057
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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