A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584822



Internal ID20957893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119362053..119364012hg38UCSC Ensembl
chr11:119232763..119234722hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381960
hg191960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227229
Samples
Known GenesUSP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584822
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