A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016659



Internal ID20583699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21355401..21356612hg38UCSC Ensembl
chr14:21823560..21824771hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381212
hg191212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494705
Supporting Variants
Samples
Known GenesSUPT16H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00078


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