A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565207



Internal ID20938278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145397833..145417140hg38UCSC Ensembl
chr5:144777396..144796703hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3819308
hg1919308
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565207
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