A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891541



Internal ID18839251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6650885..6684954hg38UCSC Ensembl
Outerchr9:6650885..6703997hg38UCSC Ensembl
Innerchr9:6650885..6684954hg19UCSC Ensembl
Outerchr9:6650885..6703997hg19UCSC Ensembl
Innerchr9:6640885..6674954hg18UCSC Ensembl
Outerchr9:6640885..6693997hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3853113
hg1953113
hg1853113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778493, essv25798367, essv25787249, essv25778674, essv25778400, essv25794397, essv25780827, essv25783848, essv25801121, essv25785464, essv25799894, essv25780885, essv25800239, essv25797985, essv25797833, essv25784704, essv25798454, essv25798005, essv25787729, essv25784253, essv25797255, essv25801661, essv25797299, essv25786848, essv25796773, essv25800307, essv25796820, essv25784944, essv25800844, essv25779292, essv25801135, essv25800889, essv25797097, essv25787712, essv25798476, essv25781986, essv25795069, essv25800628, essv25800446, essv25801205, essv25781030, essv25797632, essv25799839
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)esv3891541
Frequency
Sample Size3017
Observed Gain0
Observed Loss43
Observed Complex0
Frequencyn/a


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