A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3573364



Internal ID18354876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46113305..46707273hg38UCSC Ensembl
Innerchr17:44190671..44784639hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38593969
hg19593969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv939e212
Supporting Variantsessv9814342, essv9814345, essv9814340, essv9814334, essv9814343, essv9814341, essv9814337, essv9814332, essv9814336, essv9814335, essv9814338, essv9814331, essv9814339, essv9814330
Samples401636WR, 400789KV, 400272AE, 400949AM, 401173AI, 400333CC, 401175FA, 400093BL, 400994HJ, 400258BC, 401200BD, 400474GF, 401361GG, 401143LK
Known GenesARL17A, ARL17B, KANSL1, KANSL1-AS1, LOC644172, LRRC37A, LRRC37A2, NSF, NSFP1
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)esv3573364
Frequency
Sample Size873
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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