A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565564



Internal ID20938635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17295518..17348219hg38UCSC Ensembl
chr5:17295627..17348328hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3852702
hg1952702
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565564
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