A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451305



Internal ID22509177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89379755..89384736hg38UCSC Ensembl
chr11:89112923..89117904hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg384982
hg194982
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848337
Supporting Variants
Samples
Known GenesNOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451305
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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