A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797542



Internal ID19160022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40690593..40920099hg38UCSC Ensembl
Innerchr14:41159798..41389304hg19UCSC Ensembl
Innerchr14:40229548..40459054hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38229507
hg19229507
hg18229507
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 Human OmniExpress
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797542
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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