A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587252



Internal ID6711948
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1004666
Supporting Variants
SamplesHuRef
Known GenesYLPM1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587252
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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