A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010094



Internal ID7074159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:144077930..144212471hg38UCSC Ensembl
InnerchrX:143161036..143295577hg19UCSC Ensembl
InnerchrX:142988696..143123277hg18UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38134542
hg19134542
hg18134582
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586320
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010094
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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