A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2175n223



Internal ID22805143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65088482..65090909hg38UCSC Ensembl
chr14:65555200..65557627hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg382428
hg192428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6492987, nsv6487316
Samples
Known GenesLOC100506321, MAX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2175n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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