A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652456



Internal ID21600761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26417402..26417402hg38UCSC Ensembl
chr15:26662549..26662549hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084894, nssv17087909
SamplesHG03486, HG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652456
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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