A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645922



Internal ID21594227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21205608..21205608hg38UCSC Ensembl
chr12:21358542..21358542hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079450
SamplesHG03009
Known GenesSLCO1B1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645922
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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