A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558840



Internal ID20931911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67517803..67518655hg38UCSC Ensembl
chr5:66813631..66814483hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg38853
hg19853
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266954
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558840
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