A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587066



Internal ID7058448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:43277183..43285534hg38UCSC Ensembl
InnerchrX:43136432..43144783hg19UCSC Ensembl
InnerchrX:43021376..43029727hg18UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg388352
hg198352
hg188352
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991655
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587066
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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