A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855269



Internal ID22630204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97564469..97614266hg38UCSC Ensembl
chr11:97435469..97485266hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3849798
hg1949798
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855269
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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