A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893144



Internal ID19183964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73093559..73121767hg38UCSC Ensembl
Outerchr18:73093559..73121767hg38UCSC Ensembl
Innerchr18:70760794..70789002hg19UCSC Ensembl
Outerchr18:70760794..70789002hg19UCSC Ensembl
Innerchr18:68911774..68939982hg18UCSC Ensembl
Outerchr18:68911774..68939982hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3828209
hg1928209
hg1828209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792949
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893144
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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