A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893079



Internal ID18837213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:26912135..27610887hg38UCSC Ensembl
Outerchr18:26912135..27610887hg38UCSC Ensembl
Innerchr18:24492099..25190851hg19UCSC Ensembl
Outerchr18:24492099..25190851hg19UCSC Ensembl
Innerchr18:22746097..23444849hg18UCSC Ensembl
Outerchr18:22746097..23444849hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38698753
hg19698753
hg18698753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25793068
Samples
Known GenesAQP4-AS1, CHST9
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893079
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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