A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478579



Internal ID21136132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58279064..58292807hg38UCSC Ensembl
chr14:58745782..58759525hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3813744
hg1913744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019883
Samples
Known GenesFLJ31306
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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