A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588793



Internal ID20961864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24756142..24756902hg38UCSC Ensembl
chr10:25045071..25045831hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220966
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588793
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