A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016672



Internal ID20583712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27354380..27422109hg38UCSC Ensembl
chr14:27823586..27891315hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3867730
hg1967730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483408
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016672
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