A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605306



Internal ID21797353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20853922..20853922hg38UCSC Ensembl
chr12:21006856..21006856hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097795
Supporting Variants
Samples
Known GenesSLCO1B3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605306
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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