A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3325564



Internal ID15172546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25098456..25098475hg38UCSC Ensembl
Innerchr14:25098452..25098479hg38UCSC Ensembl
Outerchr14:25098433..25098498hg38UCSC Ensembl
chr14:25567662..25567681hg19UCSC Ensembl
Innerchr14:25567658..25567685hg19UCSC Ensembl
Outerchr14:25567639..25567704hg19UCSC Ensembl
chr14:24637502..24637521hg18UCSC Ensembl
Innerchr14:24637525..24637498hg18UCSC Ensembl
Outerchr14:24637479..24637544hg18UCSC Ensembl
Cytoband14q12
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 Variantsessv9664324
SamplesNA12873
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3325564
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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