A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582598



Internal ID20955669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66797589..66798598hg38UCSC Ensembl
chr11:66565060..66566069hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381010
hg191010
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1214n223
Supporting Variantsnssv18235836
Samples
Known GenesC11orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582598
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