A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892579



Internal ID19183399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98504373..98575338hg38UCSC Ensembl
Outerchr14:98504373..98575338hg38UCSC Ensembl
Innerchr14:98970710..99041675hg19UCSC Ensembl
Outerchr14:98970710..99041675hg19UCSC Ensembl
Innerchr14:98040463..98111428hg18UCSC Ensembl
Outerchr14:98040463..98111428hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3870966
hg1970966
hg1870966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779853, essv25780664
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892579
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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