A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016007



Internal ID20583047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105746658..105773003hg38UCSC Ensembl
chr14:106212995..106239340hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3826346
hg1926346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512502
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016007
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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