A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631329



Internal ID7018138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133134821..133160683hg38UCSC Ensembl
chr12:133711407..133737269hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3825863
hg1925863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14650394, essv14650395
SamplesNA19238, HG00108
Known GenesZNF10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631329
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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