A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859689



Internal ID22634624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94507814..94515258hg38UCSC Ensembl
chr11:94240980..94248424hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg387445
hg197445
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464721
Samples
Known GenesLOC643037
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859689
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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