A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586988



Internal ID7058370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18986104..19956456hg38UCSC Ensembl
Innerchr14:19572052..20424615hg19UCSC Ensembl
Innerchr14:18642052..19494455hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38970353
hg19852564
hg18852404
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1003217
Supporting Variants
SamplesHuRef
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEG, POTEM
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586988
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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