A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576976



Internal ID20950047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63591087..63592167hg38UCSC Ensembl
chr11:63358559..63359639hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227284
Samples
Known GenesPLA2G16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576976
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