A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079456



Internal ID21512644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21609549..21623450hg38UCSC Ensembl
chr12:21762483..21776384hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3813902
hg1913902
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667280
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079456
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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