A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892543



Internal ID19183363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:51295971..51327698hg38UCSC Ensembl
Outerchr14:51295971..51327698hg38UCSC Ensembl
Innerchr14:51762689..51794416hg19UCSC Ensembl
Outerchr14:51762689..51794416hg19UCSC Ensembl
Innerchr14:50832439..50864166hg18UCSC Ensembl
Outerchr14:50832439..50864166hg18UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3831728
hg1931728
hg1831728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786776
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892543
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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