A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160332



Internal ID21427733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129425467..129443676hg38UCSC Ensembl
chr9:132187746..132205955hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3818210
hg1918210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670471
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160332
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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