A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3574272



Internal ID18355784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:102369659..102489664hg38UCSC Ensembl
InnerchrX:101624580..101744584hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38120006
hg19120005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9828015, essv9828016, essv9828021, essv9828013, essv9828009, essv9828020, essv9828018, essv9828017, essv9828012, essv9828010, essv9828014, essv9828008, essv9828019
Samples400424LN, 400984LD, 400468OB, 400221VM, 401165SB, 400663MD, 400533BB, 401822TL, 400050RL, 400547BS, 401817MC, 400261RN, 401576WC
Known GenesNXF2, NXF2B, TCP11X2
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
Comments
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)esv3574272
Frequency
Sample Size873
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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