A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582089



Internal ID20955160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113851678..113852290hg38UCSC Ensembl
chr11:113722400..113723012hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229036
Samples
Known GenesUSP28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582089
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