A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671380



Internal ID21619685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152886745..152892275hg38UCSC Ensembl
chr5:152266305..152271835hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg385531
hg195531
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120458
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671380
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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