A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596227



Internal ID6983544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57172465..57187324hg38UCSC Ensembl
chr3:57206493..57221352hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3814860
hg1914860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11020106, essv11020105
SamplesNA18603, HG01845
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596227
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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