A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892475



Internal ID18836609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:23176509..23191859hg38UCSC Ensembl
Outerchr14:23176509..23191859hg38UCSC Ensembl
Innerchr14:23645718..23661068hg19UCSC Ensembl
Outerchr14:23645718..23661068hg19UCSC Ensembl
Innerchr14:22715558..22730908hg18UCSC Ensembl
Outerchr14:22715558..22730908hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3815351
hg1915351
hg1815351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781785
Samples
Known GenesSLC7A8
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892475
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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