A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592315



Internal ID20965386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119002225..119002393hg38UCSC Ensembl
chr11:118872935..118873103hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231784
Samples
Known GenesCCDC84
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592315
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