A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476375



Internal ID21133928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86345215..86356510hg38UCSC Ensembl
chr14:86811559..86822854hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3811296
hg1911296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476375
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