A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998156



Internal ID7081559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:53512097..53521609hg38UCSC Ensembl
InnerchrX:53539063..53548574hg19UCSC Ensembl
InnerchrX:53555788..53565299hg18UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg389513
hg199512
hg189512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586065
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998156
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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