A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587372



Internal ID20960443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43365987..43366396hg38UCSC Ensembl
chr11:43387537..43387946hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221899
Samples
Known GenesTTC17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587372
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