A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586572



Internal ID6711268
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007468
Supporting Variants
SamplesHuRef
Known GenesTGIF2LX
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586572
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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