A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511270



Internal ID20884597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96528740..96813464hg38UCSC Ensembl
chr14:96995077..97279801hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38284725
hg19284725
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185570
Samples
Known GenesPAPOLA, VRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511270
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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