A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918960



Internal ID22694182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102816780..102826311hg38UCSC Ensembl
chr10:104576537..104586068hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg389532
hg199532
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918960
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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