A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606240



Internal ID21798287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21210618..21293987hg38UCSC Ensembl
chr12:21363552..21446921hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3883370
hg1983370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108423
Supporting Variants
Samples
Known GenesSLCO1A2, SLCO1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606240
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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