A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3310578



Internal ID15157529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:169988976..169989676hg38UCSC Ensembl
Outerchr3:169988976..169989676hg38UCSC Ensembl
Innerchr3:169706764..169707464hg19UCSC Ensembl
Outerchr3:169706764..169707464hg19UCSC Ensembl
Innerchr3:171190158..171189458hg18UCSC Ensembl
Outerchr3:171189458..171190158hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38460
hg19460
hg18460
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7843516
SamplesNA19240
Known GenesSEC62
MethodSequencing
Analysismapreads
PlatformABI SOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3310578
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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