A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669486



Internal ID21617792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10002..347967hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38337966
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060072
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669486
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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