A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490462



Internal ID21148015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54089433..54090026hg38UCSC Ensembl
chr14:54556151..54556744hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020200
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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