A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891757



Internal ID18839467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12197945..12288714hg38UCSC Ensembl
Outerchr10:12196611..12327862hg38UCSC Ensembl
Innerchr10:12239944..12330713hg19UCSC Ensembl
Outerchr10:12238610..12369861hg19UCSC Ensembl
Innerchr10:12279950..12370719hg18UCSC Ensembl
Outerchr10:12278616..12409867hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38131252
hg19131252
hg18131252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789473, essv25788240, essv25789540
Samples
Known GenesCDC123
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891757
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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