A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484983



Internal ID21142536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23632493..23633880hg38UCSC Ensembl
chr14:24101702..24103089hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381388
hg191388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016744
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484983
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