A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29994



Internal ID12608188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:2614728..2776198hg38UCSC Ensembl
InnerchrX:2532769..2694239hg19UCSC Ensembl
InnerchrX:2542769..2704239hg18UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38161471
hg19161471
hg18161471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84233
SamplesHuRef
Known GenesCD99, CD99P1, LINC00102, XG, XGPY2
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29994
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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