A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668027



Internal ID21616334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187413817..187428794hg38UCSC Ensembl
chr3:187131605..187146582hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3814978
hg1914978
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131543
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668027
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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