A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585666



Internal ID20958737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78096474..78096826hg38UCSC Ensembl
chr11:77807520..77807872hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221972
Samples
Known GenesRNU6-83P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585666
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