A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019829



Internal ID20586869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57482254..57522634hg38UCSC Ensembl
chr14:57948972..57989352hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3840381
hg1940381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483843
Supporting Variants
Samples
Known GenesC14orf105
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019829
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