A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590377



Internal ID20963448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62367045..62367548hg38UCSC Ensembl
chr14:62833763..62834266hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237191
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590377
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