A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893110



Internal ID19183930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:61112818..61146485hg38UCSC Ensembl
Outerchr18:61112818..61146485hg38UCSC Ensembl
Innerchr18:58780051..58813718hg19UCSC Ensembl
Outerchr18:58780051..58813718hg19UCSC Ensembl
Innerchr18:56931031..56964698hg18UCSC Ensembl
Outerchr18:56931031..56964698hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3833668
hg1933668
hg1833668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790828, essv25791912
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893110
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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