A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616061



Internal ID21808108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65059752..65059843hg38UCSC Ensembl
chr14:65526470..65526561hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033041
Supporting Variants
Samples
Known GenesCHURC1-FNTB, FNTB, MAX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616061
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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