A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893107



Internal ID19183927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:55878232..56046106hg38UCSC Ensembl
Outerchr18:55878232..56046106hg38UCSC Ensembl
Innerchr18:53545463..53713337hg19UCSC Ensembl
Outerchr18:53545463..53713337hg19UCSC Ensembl
Innerchr18:51696461..51864335hg18UCSC Ensembl
Outerchr18:51696461..51864335hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38167875
hg19167875
hg18167875
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789407
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893107
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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