A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481742



Internal ID21139295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20517668..20519342hg38UCSC Ensembl
chr14:20985827..20987501hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381675
hg191675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481742
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