A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923254



Internal ID22698480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16671260..16954786hg38UCSC Ensembl
chr10:16713259..16996785hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38283527
hg19283527
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369263
Samples
Known GenesCUBN, RSU1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923254
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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