A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581264



Internal ID20954335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19233533..19233991hg38UCSC Ensembl
chr11:19255080..19255538hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218900
Samples
Known GenesE2F8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581264
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