A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892494



Internal ID19183314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:30770756..30848428hg38UCSC Ensembl
Outerchr14:30770756..30848428hg38UCSC Ensembl
Innerchr14:31239962..31317634hg19UCSC Ensembl
Outerchr14:31239962..31317634hg19UCSC Ensembl
Innerchr14:30309713..30387385hg18UCSC Ensembl
Outerchr14:30309713..30387385hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3877673
hg1977673
hg1877673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790422
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892494
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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