A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484411



Internal ID21141964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22918194..22921612hg38UCSC Ensembl
chr14:23387403..23390821hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383419
hg193419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016711
Samples
Known GenesPRMT5, RBM23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484411
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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