A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593934



Internal ID20967005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18668850..18669640hg38UCSC Ensembl
chr10:18957779..18958569hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225311
Samples
Known GenesARL5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593934
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