A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893058



Internal ID19183878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1306067..1574273hg38UCSC Ensembl
Outerchr18:1306067..1574273hg38UCSC Ensembl
Innerchr18:1306068..1574274hg19UCSC Ensembl
Outerchr18:1306068..1574274hg19UCSC Ensembl
Innerchr18:1296068..1564274hg18UCSC Ensembl
Outerchr18:1296068..1564274hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38268207
hg19268207
hg18268207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792664
Samples
Known GenesLINC00470
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893058
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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