A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579876



Internal ID20952947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124871648..124873616hg38UCSC Ensembl
chr10:126560217..126562185hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381969
hg191969
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579876
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