A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596322



Internal ID21544930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102885490..102885828hg38UCSC Ensembl
chr10:104645247..104645585hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068463
SamplesHG00732
Known GenesAS3MT, C10orf32-ASMT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596322
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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