A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1n207



Internal ID22815252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172409041..172422820hg38UCSC Ensembl
chr1:172378181..172391960hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3813780
hg1913780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5670523, nsv5669770
Samples
Known GenesC1orf105, DNM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)dgv1n207
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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