A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9786616



Internal ID18311095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:157803396..157861620hg38UCSC Ensembl
Innerchr7:157596088..157654312hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3858225
hg1958225
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3576493
Supporting Variants
Samples400926LJ
Known GenesLOC100506585, PTPRN2
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=46
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9786616
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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