A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083928



Internal ID21435623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28298425..28623514hg38UCSC Ensembl
chr15:28543571..28868660hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38325090
hg19325090
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671633
Supporting Variants
SamplesHG00731
Known GenesGOLGA8F, GOLGA8G, HERC2, MIR4509-1, MIR4509-2, MIR4509-3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083928
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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