A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256789



Internal ID21398193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82344935..82453182hg38UCSC Ensembl
chr15:83013616..83121878hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38108248
hg19108263
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730190
Supporting Variants
SamplesHG00513
Known GenesGOLGA6L20, GOLGA6L9, UBE2Q2P2, UBE2Q2P3
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256789
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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