A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661865



Internal ID21610170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38047046..38047046hg38UCSC Ensembl
chr15:38339247..38339247hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094430
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661865
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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