A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492209



Internal ID21149762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:40321305..40330826hg38UCSC Ensembl
chr14:40790509..40800030hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg389522
hg199522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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