A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554486



Internal ID20927580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69220779..69220993hg38UCSC Ensembl
chr3:69269930..69270144hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262856
Samples
Known GenesFRMD4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554486
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