A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482825



Internal ID21140378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20819772..20821074hg38UCSC Ensembl
chr14:21287931..21289233hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381303
hg191303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482825
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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