A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758894



Internal ID9634353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135066857..135364390hg38UCSC Ensembl
InnerchrX:134200887..134498315hg19UCSC Ensembl
InnerchrX:134028553..134325981hg18UCSC Ensembl
InnerchrX:133926407..134223835hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38297534
hg19297429
hg18297429
hg17297429
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758592
SamplesNA18633
Known GenesCXorf48, LINC00087, LINC00633, LOC100287728, ZNF449, ZNF75D
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)esv2758894
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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