A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792949



Internal ID19180965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73093559..73121767hg38UCSC Ensembl
Innerchr18:70760794..70789002hg19UCSC Ensembl
Innerchr18:68911774..68939982hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3828209
hg1928209
hg1828209
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893144
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792949
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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