A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891572



Internal ID19185968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12013711..12096410hg38UCSC Ensembl
Outerchr9:12010374..12115049hg38UCSC Ensembl
Innerchr9:12013711..12096410hg19UCSC Ensembl
Outerchr9:12010374..12115049hg19UCSC Ensembl
Innerchr9:12003711..12086410hg18UCSC Ensembl
Outerchr9:12000374..12105049hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38104676
hg19104676
hg18104676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798765, essv25796049, essv25780685, essv25801129, essv25780333, essv25784219, essv25787550, essv25799022, essv25786756, essv25778774, essv25778874, essv25799373, essv25782285, essv25798475, essv25800802, essv25799660, essv25797967, essv25798230, essv25778238, essv25781488, essv25780135, essv25799491, essv25779005, essv25799002, essv25783065, essv25798710, essv25787748, essv25786317, essv25798340, essv25781050, essv25785884
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)esv3891572
Frequency
Sample Size3017
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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