A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3350518



Internal ID15163268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15906871..15906871hg38UCSC Ensembl
Innerchr6:15906870..15906872hg38UCSC Ensembl
Outerchr6:15906821..15906921hg38UCSC Ensembl
chr6:15907102..15907102hg19UCSC Ensembl
Innerchr6:15907101..15907103hg19UCSC Ensembl
Outerchr6:15907052..15907152hg19UCSC Ensembl
chr6:16015081..16015081hg18UCSC Ensembl
Innerchr6:16015082..16015080hg18UCSC Ensembl
Outerchr6:16015031..16015131hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38743
hg19743
hg18743
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8653444, essv8653443, essv8653445
SamplesNA12891, NA12878, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3350518
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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