A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781201



Internal ID19176202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40709553..40917801hg38UCSC Ensembl
Innerchr14:41178758..41387006hg19UCSC Ensembl
Innerchr14:40248508..40456756hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38208249
hg19208249
hg18208249
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892511
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=33
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781201
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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