A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586909



Internal ID7058291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:12976299..12977121hg38UCSC Ensembl
InnerchrX:12994418..12995240hg19UCSC Ensembl
InnerchrX:12904339..12905161hg18UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38823
hg19823
hg18823
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1002384
Supporting Variants
SamplesHuRef
Known GenesTMSB4X
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586909
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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