A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3583537



Internal ID18365049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54819186..54836206hg38UCSC Ensembl
Innerchr19:55330641..55347661hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3817021
hg1917021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9818261, essv9818267, essv9818260, essv9818259, essv9818263, essv9818258, essv9818264, essv9818256, essv9818265, essv9818257, essv9818268, essv9818262
Samples401036WS, 401719RL, 400641WJ, 401019MP, 401634CH, 401975VD, 400669LD, 401038LN, 401406KF, 401039PA, 401894PD, 401040KM
Known GenesKIR2DS4, KIR3DL1
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)esv3583537
Frequency
Sample Size873
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer