A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505488



Internal ID20878758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99637558..99643850hg38UCSC Ensembl
chr14:100103895..100110187hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg386293
hg196293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505488
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