A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563556



Internal ID20936627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132552049..132552751hg38UCSC Ensembl
chr5:131887741..131888443hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563556
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