A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541364



Internal ID20914646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37278317..37279813hg38UCSC Ensembl
chr3:37319808..37321304hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381497
hg191497
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260000
Samples
Known GenesGOLGA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541364
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