A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091716



Internal ID21488453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37982480..37982480hg38UCSC Ensembl
chr15:38274681..38274681hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647483
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091716
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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