A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9828062



Internal ID18341221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:103917015..103966774hg38UCSC Ensembl
InnerchrX:103171609..103221347hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3849760
hg1949739
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3577011
Supporting Variants
Samples401832MC
Known GenesMIR1256, TMSB15B
MethodSNP array
AnalysisWe used four separate algorithms to detect CNVs; Affymetrix Chromosome Analysis Suite (ChAS), iPattern, Nexus and Partek. Our primary analysis was performed based on ChAS CNV calls, which were then supported using the remaining three algorithms to construct a confidence set of CNVs. For all algorithms, we have used 8 probes and >1kb as a base line cutoff for CNV detection.
PlatformAffymetrix CytoScan HD 2.7M array
CommentsNumber of probes=44
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9828062
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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