A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3594879



Internal ID6635154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65856..151558hg38UCSC Ensembl
chr3:107539..193241hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3885703
hg1985703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10896248, essv10896249
SamplesHG01768, NA18499
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3594879
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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