A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586391



Internal ID21534944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123857542..123857649hg38UCSC Ensembl
chr10:125617058..125617165hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066727
SamplesHG01505
Known GenesCPXM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586391
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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