A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3308692



Internal ID15155641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14657156..14657157hg38UCSC Ensembl
Innerchr6:14657129..14657184hg38UCSC Ensembl
Outerchr6:14657128..14657185hg38UCSC Ensembl
chr6:14657387..14657388hg19UCSC Ensembl
Innerchr6:14657360..14657415hg19UCSC Ensembl
Outerchr6:14657359..14657416hg19UCSC Ensembl
chr6:14765366..14765367hg18UCSC Ensembl
Innerchr6:14765394..14765339hg18UCSC Ensembl
Outerchr6:14765338..14765395hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38128
hg19128
hg18128
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7838041, essv7837889
SamplesNA12878, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3308692
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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