A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854416



Internal ID22629351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81198866..81206902hg38UCSC Ensembl
chr11:80909909..80917945hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg388037
hg198037
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv276n209
Supporting Variantsnssv17465126
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854416
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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