A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109395



Internal ID22018628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28326290..28465083hg38UCSC Ensembl
chr15:28571436..28710229hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38138794
hg19138794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607424
Samples
Known GenesGOLGA8F, GOLGA8G, MIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109395
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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