A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010013



Internal ID7059707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135703990..135900575hg38UCSC Ensembl
InnerchrX:134837705..134982734hg19UCSC Ensembl
InnerchrX:134665371..134810400hg18UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38196586
hg19145030
hg18145030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586397
SamplesHuRef
Known GenesCT45A1, CT45A2, CT45A3, CT45A4, CT45A5, CT45A6, SAGE1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010013
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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