A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479177



Internal ID21136730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78938251..79002486hg38UCSC Ensembl
chr14:79404594..79468829hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3864236
hg1964236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020931
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479177
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