A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856361



Internal ID22631296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34489207..34491506hg38UCSC Ensembl
chr11:34510754..34513053hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454049
Samples
Known GenesELF5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856361
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