A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892456



Internal ID19183276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18223945..18460568hg38UCSC Ensembl
Outerchr14:18223945..18594126hg38UCSC Ensembl
Innerchr14:19000422..19237045hg19UCSC Ensembl
Outerchr14:19000422..19370603hg19UCSC Ensembl
Innerchr14:18070422..18307045hg18UCSC Ensembl
Outerchr14:18070422..18440603hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38370182
hg19370182
hg18370182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790400, essv25792367, essv25792081, essv25790118, essv25791193, essv25790007, essv25792012, essv25792074, essv25792388, essv25792407, essv25790067, essv25792144, essv25792139, essv25792266, essv25790585, essv25792441, essv25790452, essv25790553, essv25791359, essv25792178, essv25792219, essv25790864, essv25792094, essv25790506, essv25790148, essv25790738, essv25790445, essv25790411, essv25791619, essv25791278, essv25792133, essv25792160, essv25792272, essv25790524
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892456
Frequency
Sample Size3017
Observed Gain34
Observed Loss0
Observed Complex0
Frequencyn/a


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