A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671840



Internal ID21620148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46870366..47099487hg38UCSC Ensembl
chr1:47336038..47565159hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38229122
hg19229122
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065955
Samples
Known GenesCYP4A11, CYP4X1, CYP4Z1, CYP4Z2P
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671840
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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