A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8932022



Internal ID14338613
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 StatusS
Merged Variantsesv3328257
Supporting Variants
SamplesNA18853
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8932022
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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