A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911799



Internal ID22687014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16559383..16559463hg38UCSC Ensembl
chr11:16580930..16581010hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911799
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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