A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861840



Internal ID22636775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96903214..96914091hg38UCSC Ensembl
chr11:96774214..96785091hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3810878
hg1910878
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455103
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861840
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