A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650786



Internal ID21599091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57841458..57841458hg38UCSC Ensembl
chr15:58133656..58133656hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086186
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650786
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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