A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666974



Internal ID21615279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82360483..82517398hg38UCSC Ensembl
chr15:83029208..83186384hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38156916
hg19157177
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085413
SamplesHG00513
Known GenesCSPG4P8, GOLGA6L20, GOLGA6L9, LOC727751, LOC80154, UBE2Q2P2, UBE2Q2P3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666974
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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