A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611680



Internal ID6998586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167934707..167976031hg38UCSC Ensembl
chr6:168335387..168376711hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3841325
hg1941325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12643900, essv12643898, essv12643907, essv12643897, essv12643905, essv12643903, essv12643893, essv12643904, essv12643896, essv12643894, essv12643906, essv12643899, essv12643895, essv12643891, essv12643902, essv12643892, essv12643901
SamplesHG01438, HG01773, HG02231, NA20294, HG00356, NA20589, HG01761, HG00232, NA12815, NA19774, NA11894, NA12249, NA06985, HG01375, HG01395, HG01509, HG01786
Known GenesHGC6.3, MLLT4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611680
Frequency
Sample Size2504
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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