A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194924



Internal ID20761964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105740301..105755700hg38UCSC Ensembl
chr14:106206638..106222037hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3815400
hg1915400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500758
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194924
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00976


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