A curated catalogue of human genomic structural variation




Variant Details

Variant: esv32737



Internal ID1683859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71263986..72546603hg19UCSC Ensembl
Innerchr10:70933992..72216609hg18UCSC Ensembl
Innerchr10:70933992..72216609hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain+Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv96066, essv94691, essv95630, essv99350, essv99363, essv94223, essv98040, essv93626, essv99282, essv98557, essv99073, essv95988, essv98301, essv97538, essv97060, essv100351, essv99906
Samples21616, 21972, 21938, 22085, 21817, 21841, 22259, 21791, 21772, 22335, 22394, 22127, 22086, 22275, 22300
Known GenesADAMTS14, AIFM2, C10orf27, C10orf35, COL13A1, EIF4EBP2, H2AFY2, KIAA1274, LRRC20, NEUROG3, NODAL, NPFFR1, PPA1, PRF1, SAR1A, TSPAN15, TYSND1
Method
Analysis
PlatformAgilent-015366 Custom Human 244K CGH Microarray
Comments
Referencede_Smith_et_al_2007
Pubmed ID17666407
Accession Number(s)esv32737
Frequency
Sample Size51
Observed Gain15
Observed Loss2
Observed Complex0
Frequencyn/a


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