A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581013



Internal ID20954084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108404383..108433685hg38UCSC Ensembl
chr11:108275110..108304412hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3829303
hg1929303
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225756
Samples
Known GenesC11orf65
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581013
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