A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494451



Internal ID21152004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58613772..58614642hg38UCSC Ensembl
chr14:59080490..59081360hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019902
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494451
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer