A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664654



Internal ID21612959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53902574..54093373hg38UCSC Ensembl
chr13:54476709..54667508hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38190800
hg19190800
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095363
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664654
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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