A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007468



Internal ID6719582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:89201856..90005924hg38UCSC Ensembl
InnerchrX:88456855..89260923hg19UCSC Ensembl
InnerchrX:88343511..89147579hg18UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38804069
hg19804069
hg18804069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586572
SamplesHuRef
Known GenesTGIF2LX
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007468
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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