A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662953



Internal ID21611258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50229239..50229239hg38UCSC Ensembl
chr15:50521436..50521436hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086736
SamplesHG02818
Known GenesSLC27A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662953
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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