A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004741



Internal ID7069837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151555480..151563187hg38UCSC Ensembl
InnerchrX:150723952..150731659hg19UCSC Ensembl
InnerchrX:150474608..150482315hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg387708
hg197708
hg187708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586531
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004741
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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