A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995876



Internal ID7080186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:123817230..123818917hg38UCSC Ensembl
InnerchrX:122951080..122952767hg19UCSC Ensembl
InnerchrX:122778761..122780448hg18UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg381688
hg191688
hg181688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586641
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995876
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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