A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850019



Internal ID22624954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111520156..111525880hg38UCSC Ensembl
chr11:111390881..111396605hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg385725
hg195725
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462053
Samples
Known GenesC11orf88
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850019
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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