A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989473



Internal ID7076174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:30788566..30806771hg38UCSC Ensembl
InnerchrX:30806683..30824888hg19UCSC Ensembl
InnerchrX:30716604..30734809hg18UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3818206
hg1918206
hg1818206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586180
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989473
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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