A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3236273



Internal ID22373535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63817238..63822357hg38UCSC Ensembl
chr11:63584710..63589829hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385120
hg195120
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359801
SamplesHG00732
Known GenesC11orf84
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3236273
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer