A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091092



Internal ID21432348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84270068..84399999hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38129932
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666300
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091092
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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