A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494123



Internal ID21151676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61188971..61194433hg38UCSC Ensembl
chr14:61655689..61661151hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg385463
hg195463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494123
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