A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767306



Internal ID20543166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90267333..90267333hg38UCSC Ensembl
chr11:90000501..90000501hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262583
Samples
Known GenesDISC1FP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767306
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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