A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3328257



Internal ID15175242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109886567..109886597hg38UCSC Ensembl
Innerchr6:109886579..109886583hg38UCSC Ensembl
Outerchr6:109886549..109886615hg38UCSC Ensembl
chr6:110207770..110207800hg19UCSC Ensembl
Innerchr6:110207782..110207786hg19UCSC Ensembl
Outerchr6:110207752..110207818hg19UCSC Ensembl
chr6:110314463..110314493hg18UCSC Ensembl
Innerchr6:110314479..110314475hg18UCSC Ensembl
Outerchr6:110314445..110314511hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38276
hg19276
hg18276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8932021, essv8932022, essv8932020, essv8932019, essv8932018
SamplesNA18912, NA18853, NA19225, NA18523, NA19147
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3328257
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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