A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856346



Internal ID22631281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101139986..101147985hg38UCSC Ensembl
chr11:101010717..101018716hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455640
Samples
Known GenesLOC101054525
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856346
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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