A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890885



Internal ID19185281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76682109..76691135hg38UCSC Ensembl
Outerchr6:76682109..76693824hg38UCSC Ensembl
Innerchr6:77391826..77400852hg19UCSC Ensembl
Outerchr6:77391826..77403541hg19UCSC Ensembl
Innerchr6:77448545..77457571hg18UCSC Ensembl
Outerchr6:77448545..77460260hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3811716
hg1911716
hg1811716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797653, essv25781857, essv25796479, essv25787686, essv25778696, essv25796083
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890885
Frequency
Sample Size3017
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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