A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596450



Internal ID6983765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67145428..67286310hg38UCSC Ensembl
chr3:67195852..67336734hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38140883
hg19140883
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11030925, essv11030923, essv11030924, essv11030922, essv11030927, essv11030926
SamplesHG01069, HG01398, HG01200, HG04017, HG04026, HG04023
Known GenesMIR4272
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596450
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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