A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848337



Internal ID22623272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89379755..89384736hg38UCSC Ensembl
chr11:89112923..89117904hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg384982
hg194982
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467913, nssv17451305
Samples
Known GenesNOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848337
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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