A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082932



Internal ID21512643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48199211..48206661hg38UCSC Ensembl
chr13:48773347..48780797hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg387451
hg197451
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672482
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082932
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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