A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668631



Internal ID21616936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:242141116..242183528hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3842413
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17112836
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668631
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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