A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061202



Internal ID18803733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669231..15714929hg38UCSC Ensembl
Innerchr19:15780041..15825739hg19UCSC Ensembl
Innerchr19:15641041..15686739hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3845699
hg1945699
hg1845699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3446n100
Supporting Variantsnssv3564917, nssv3564911, nssv3564876, nssv3564886, nssv3564892, nssv3564915, nssv3564881, nssv3564880, nssv3564925, nssv3564889, nssv3564909, nssv3564893, nssv3564877, nssv3564900, nssv3564901, nssv3564879, nssv3564924, nssv3564888, nssv3564891, nssv3564908, nssv3564899, nssv3564918, nssv3564885, nssv3564896, nssv3564894, nssv3564916, nssv3564919, nssv3564913, nssv3564906, nssv3564898, nssv3564883, nssv3564878, nssv3564884, nssv3564904, nssv3564923, nssv3564882, nssv3564905, nssv3564914, nssv3564895, nssv3564910, nssv3564907, nssv3564887, nssv3564902, nssv3564920, nssv3564890, nssv3564903, nssv3564922, nssv3564897, nssv3564921, nssv3564912
Samples
Known GenesCYP4F12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061202
Frequency
Sample Size29084
Observed Gain50
Observed Loss0
Observed Complex0
Frequencyn/a


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