A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593401



Internal ID20966472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57730381..57731238hg38UCSC Ensembl
chr11:57497853..57498710hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38858
hg19858
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225953
Samples
Known GenesTMX2, TMX2-CTNND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593401
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