A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586087



Internal ID7057469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:92284007..93120368hg38UCSC Ensembl
InnerchrX:91539006..92375367hg19UCSC Ensembl
InnerchrX:91425662..92262023hg18UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38836362
hg19836362
hg18836362
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001030
Supporting Variants
SamplesHuRef
Known GenesPCDH11X
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586087
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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