A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019714



Internal ID20586754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49904832..49914525hg38UCSC Ensembl
chr14:50371550..50381243hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg389694
hg199694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019714
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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