A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662396



Internal ID21610701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38988040..38988040hg38UCSC Ensembl
chr13:39562177..39562177hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080190
SamplesHG00513
Known GenesSTOML3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662396
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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