A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591503



Internal ID20964574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47736432..47737524hg38UCSC Ensembl
chr11:47757984..47759076hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381093
hg191093
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1037n223
Supporting Variantsnssv18236290
Samples
Known GenesFNBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591503
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