A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492380



Internal ID21149933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34593176..34707309hg38UCSC Ensembl
chr14:35062382..35176515hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38114134
hg19114134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195369
Samples
Known GenesSNX6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492380
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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