A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800390



Internal ID19167357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27401638..27499536hg38UCSC Ensembl
Innerchr14:27870844..27968742hg19UCSC Ensembl
Innerchr14:26940684..27038582hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3897899
hg1997899
hg1897899
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892488
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800390
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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