A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892479



Internal ID19183299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:25251826..25388598hg38UCSC Ensembl
Outerchr14:25214652..25388598hg38UCSC Ensembl
Innerchr14:25721032..25857804hg19UCSC Ensembl
Outerchr14:25683858..25857804hg19UCSC Ensembl
Innerchr14:24790872..24927644hg18UCSC Ensembl
Outerchr14:24753698..24927644hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38173947
hg19173947
hg18173947
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790123, essv25790018, essv25793027, essv25790149
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892479
Frequency
Sample Size3017
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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