A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576838



Internal ID20949909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118714450..118716312hg38UCSC Ensembl
chr11:118585159..118587021hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381863
hg191863
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235007
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576838
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