A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638417



Internal ID21586722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36483390..36483390hg38UCSC Ensembl
chr9:36483387..36483387hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161743
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638417
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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