A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016554



Internal ID20583594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20426886..20440545hg38UCSC Ensembl
chr14:20895045..20908704hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3813660
hg1913660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488450
Supporting Variants
Samples
Known GenesKLHL33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016554
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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