A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9785914



Internal ID18311677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148308151..148315985hg38UCSC Ensembl
Innerchr7:148005243..148013077hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg387835
hg197835
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3572287
Supporting Variants
Samples400942HR
Known GenesCNTNAP2, MIR548T
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=24
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9785914
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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