A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891763



Internal ID19186159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14962453..15012424hg38UCSC Ensembl
Outerchr10:14948370..15018884hg38UCSC Ensembl
Innerchr10:15004452..15054423hg19UCSC Ensembl
Outerchr10:14990369..15060883hg19UCSC Ensembl
Innerchr10:15044458..15094429hg18UCSC Ensembl
Outerchr10:15030375..15100889hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3870515
hg1970515
hg1870515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788389, essv25790885, essv25792943, essv25792486, essv25787918, essv25789125, essv25792360, essv25789121
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891763
Frequency
Sample Size3017
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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