A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3384413



Internal ID15231383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103263401..103263420hg38UCSC Ensembl
Innerchr14:103263397..103263424hg38UCSC Ensembl
Outerchr14:103263378..103263443hg38UCSC Ensembl
chr14:103729738..103729757hg19UCSC Ensembl
Innerchr14:103729734..103729761hg19UCSC Ensembl
Outerchr14:103729715..103729780hg19UCSC Ensembl
chr14:102799491..102799510hg18UCSC Ensembl
Innerchr14:102799514..102799487hg18UCSC Ensembl
Outerchr14:102799468..102799533hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9667624
SamplesNA19143
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3384413
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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