A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027531



Internal ID21936874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21205311..21206561hg38UCSC Ensembl
chr12:21358245..21359495hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg381251
hg191251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613789
Samples
Known GenesSLCO1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027531
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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