A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670558



Internal ID21618863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73657970..73660146hg38UCSC Ensembl
chr10:75417728..75419904hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg382177
hg192177
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071407
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670558
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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