A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3444163



Internal ID15291116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106010684..106012682hg38UCSC Ensembl
Innerchr6:106011682..106011684hg38UCSC Ensembl
Outerchr6:106009684..106013682hg38UCSC Ensembl
chr6:106458559..106460557hg19UCSC Ensembl
Innerchr6:106459557..106459559hg19UCSC Ensembl
Outerchr6:106457559..106461557hg19UCSC Ensembl
chr6:106565252..106567250hg18UCSC Ensembl
Innerchr6:106566252..106566250hg18UCSC Ensembl
Outerchr6:106564252..106568250hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381999
hg191999
hg181999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3610e59
Supporting Variantsessv8695011
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3444163
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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