A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892636



Internal ID19183456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17159056..17184208hg38UCSC Ensembl
Outerchr1:17159056..17184208hg38UCSC Ensembl
Innerchr1:17485551..17510703hg19UCSC Ensembl
Outerchr1:17485551..17510703hg19UCSC Ensembl
Innerchr1:17358138..17383290hg18UCSC Ensembl
Outerchr1:17358138..17383290hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3825153
hg1925153
hg1825153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786663, essv25782334, essv25782507, essv25798477, essv25782733, essv25781376
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892636
Frequency
Sample Size3017
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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