A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182902



Internal ID20749942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99211654..99226232hg38UCSC Ensembl
chr14:99677991..99692569hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3814579
hg1914579
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498487
Supporting Variants
Samples
Known GenesBCL11B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182902
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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