A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892511



Internal ID19183331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40709553..40917801hg38UCSC Ensembl
Outerchr14:40690593..40920099hg38UCSC Ensembl
Innerchr14:41178758..41387006hg19UCSC Ensembl
Outerchr14:41159798..41389304hg19UCSC Ensembl
Innerchr14:40248508..40456756hg18UCSC Ensembl
Outerchr14:40229548..40459054hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38229507
hg19229507
hg18229507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781201, essv25799232, essv25797542
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892511
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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