A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582543



Internal ID21774586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96399530..96399868hg38UCSC Ensembl
chr11:96132694..96133032hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109201
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582543
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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