A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893076



Internal ID19183896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14194215..14242305hg38UCSC Ensembl
Outerchr18:14194215..14281865hg38UCSC Ensembl
Innerchr18:14194214..14242304hg19UCSC Ensembl
Outerchr18:14194214..14281864hg19UCSC Ensembl
Innerchr18:14184214..14232304hg18UCSC Ensembl
Outerchr18:14184214..14271864hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3887651
hg1987651
hg1887651
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791079, essv25785801
Samples
Known GenesANKRD20A5P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893076
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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