A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988564



Internal ID7060511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:142226301..142232936hg38UCSC Ensembl
InnerchrX:141314087..141320722hg19UCSC Ensembl
InnerchrX:141141753..141148388hg18UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg386636
hg196636
hg186636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586362
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988564
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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