A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016059



Internal ID20583099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21888498..22496897hg38UCSC Ensembl
chr14:22356678..22965882hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38608400
hg19609205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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