A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018010



Internal ID20585050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37176659..37182410hg38UCSC Ensembl
chr14:37645864..37651615hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg385752
hg195752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493026
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018010
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