A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3441435



Internal ID15288388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11490433..11492431hg38UCSC Ensembl
Innerchr6:11491431..11491433hg38UCSC Ensembl
Outerchr6:11489433..11493431hg38UCSC Ensembl
chr6:11490666..11492664hg19UCSC Ensembl
Innerchr6:11491664..11491666hg19UCSC Ensembl
Outerchr6:11489666..11493664hg19UCSC Ensembl
chr6:11598652..11600650hg18UCSC Ensembl
Innerchr6:11599652..11599650hg18UCSC Ensembl
Outerchr6:11597652..11601650hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg381999
hg191999
hg181999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3447e59
Supporting Variantsessv8695028
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3441435
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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