A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581802



Internal ID20954873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22745877..22795248hg38UCSC Ensembl
chr14:23215086..23264457hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3849372
hg1949372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230358
Samples
Known GenesOXA1L, SLC7A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581802
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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