A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925266



Internal ID22700493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:39507177..39517464hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3810288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925266
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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