A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580468



Internal ID20953539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22908697..22910205hg38UCSC Ensembl
chr14:23377906..23379414hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381509
hg191509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227386
Samples
Known GenesRBM23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580468
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