A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647483



Internal ID21595788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37982480..37982480hg38UCSC Ensembl
chr15:38274681..38274681hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086969, nssv17091716, nssv17092500
SamplesNA19238, HG00731, NA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647483
Frequency
Sample Size35
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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