A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556459



Internal ID20929530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138030222..138031019hg38UCSC Ensembl
chr5:137365911..137366708hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266793
Samples
Known GenesFAM13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556459
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