A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925281



Internal ID22700508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36601663..36879150hg38UCSC Ensembl
chr11:36623213..36900700hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38277488
hg19277488
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368863
Samples
Known GenesC11orf74
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925281
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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