A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926729



Internal ID22701956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33700011..33700063hg38UCSC Ensembl
chr11:33721557..33721609hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354253
Samples
Known GenesC11orf91
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926729
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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