A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577448



Internal ID20950519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73910755..73911471hg38UCSC Ensembl
chr11:73621800..73622516hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220010
Samples
Known GenesPAAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577448
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