A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488450



Internal ID21146003
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 StatusM
Merged Variants
Supporting Variantsnssv18016554
Samples
Known GenesKLHL33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488450
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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