A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580955



Internal ID20954026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102274928..102276059hg38UCSC Ensembl
chr10:104034685..104035816hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381132
hg191132
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228821
Samples
Known GenesGBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580955
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