A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866752



Internal ID22641687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37490060..37492533hg38UCSC Ensembl
chr11:37511610..37514083hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382474
hg192474
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866752
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