A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617132



Internal ID21809179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46896666..46915975hg38UCSC Ensembl
chr12:47290449..47309758hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3819310
hg1919310
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617132
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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