A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3576384



Internal ID18704582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75724795..75734907hg38UCSC Ensembl
Innerchr7:75354113..75364225hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3810113
hg1910113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1926e212
Supporting Variantsessv9784153, essv9784154, essv9784152
Samples400705KK, 400681MC, 400540BM
Known GenesHIP1
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)esv3576384
Frequency
Sample Size873
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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