A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585000



Internal ID20958071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54862329..54863136hg38UCSC Ensembl
chr14:55329047..55329854hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237779
Samples
Known GenesGCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585000
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