A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020704



Internal ID20587744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64733079..64735494hg38UCSC Ensembl
chr14:65199797..65202212hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg382416
hg192416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492638
Supporting Variants
Samples
Known GenesPLEKHG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020704
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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