A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992364



Internal ID6728326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155560509..155561031hg38UCSC Ensembl
InnerchrX:154790170..154790692hg19UCSC Ensembl
InnerchrX:154443364..154443886hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38523
hg19523
hg18523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586718
SamplesHuRef
Known GenesTMLHE
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992364
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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