A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3390013



Internal ID15236980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166285445..166285821hg38UCSC Ensembl
Innerchr6:166285445..166285821hg38UCSC Ensembl
Outerchr6:166283761..166287569hg38UCSC Ensembl
chr6:166698933..166699309hg19UCSC Ensembl
Innerchr6:166698933..166699309hg19UCSC Ensembl
Outerchr6:166697249..166701057hg19UCSC Ensembl
chr6:166618923..166619299hg18UCSC Ensembl
Innerchr6:166618923..166619299hg18UCSC Ensembl
Outerchr6:166617239..166621047hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38377
hg19377
hg18377
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3709e59
Supporting Variantsessv8652313
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3390013
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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