A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234917



Internal ID20801957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122939059..122940355hg38UCSC Ensembl
chr11:122809767..122811063hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg381297
hg191297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584704
Supporting Variants
Samples
Known GenesC11orf63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234917
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer