A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670523



Internal ID21618828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172411956..172422820hg38UCSC Ensembl
chr1:172381096..172391960hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3810865
hg1910865
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1n207
Supporting Variantsnssv17061922
Samples
Known GenesC1orf105, DNM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670523
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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