A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3414756



Internal ID15261715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16950468..16950881hg38UCSC Ensembl
Innerchr6:16950468..16950881hg38UCSC Ensembl
Outerchr6:16950415..16951350hg38UCSC Ensembl
chr6:16950699..16951112hg19UCSC Ensembl
Innerchr6:16950699..16951112hg19UCSC Ensembl
Outerchr6:16950646..16951581hg19UCSC Ensembl
chr6:17058678..17059091hg18UCSC Ensembl
Innerchr6:17058678..17059091hg18UCSC Ensembl
Outerchr6:17058625..17059560hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38414
hg19414
hg18414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8652323
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3414756
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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