A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649464



Internal ID21597769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66309094..66309094hg38UCSC Ensembl
chr15:66601432..66601432hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081558
SamplesNA20847
Known GenesDIS3L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649464
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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