A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004666



Internal ID6716789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74763488..74764248hg38UCSC Ensembl
Innerchr14:75230191..75230951hg19UCSC Ensembl
Innerchr14:74299944..74300704hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38761
hg19761
hg18761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587252
SamplesHuRef
Known GenesYLPM1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004666
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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