A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579825



Internal ID20952896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102122728..102123816hg38UCSC Ensembl
chr11:101993459..101994547hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381089
hg191089
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235220
Samples
Known GenesYAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579825
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