A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890897



Internal ID19185293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80564619..80579673hg38UCSC Ensembl
Outerchr6:80564619..80579673hg38UCSC Ensembl
Innerchr6:81274336..81289390hg19UCSC Ensembl
Outerchr6:81274336..81289390hg19UCSC Ensembl
Innerchr6:81331055..81346109hg18UCSC Ensembl
Outerchr6:81331055..81346109hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3815055
hg1915055
hg1815055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797254
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890897
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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