A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656859



Internal ID21605164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21277270..21277270hg38UCSC Ensembl
chr12:21430204..21430204hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079451
SamplesHG03683
Known GenesSLCO1A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656859
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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