A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865992



Internal ID22640927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41978010..41979609hg38UCSC Ensembl
chr11:41999560..42001159hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462485, nssv17454798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865992
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