A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577796



Internal ID20950867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5318526..5345924hg38UCSC Ensembl
chr10:5360489..5387887hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3827399
hg1927399
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230120
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577796
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