A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577963



Internal ID20951034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117152994..117153629hg38UCSC Ensembl
chr11:117023710..117024345hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38636
hg19636
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222678
Samples
Known GenesPAFAH1B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577963
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