A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2238n100



Internal ID22788325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20305889..22300068hg38UCSC Ensembl
chr15:20511142..22588019hg19UCSC Ensembl
chr15:18771156..20089383hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381994180
hg192076878
hg181318228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045023, nsv1053787, nsv1046154, nsv1042802, nsv1035528, nsv1035175, nsv1038126, nsv1051168, nsv1049828, nsv1047580, nsv1040949, nsv1042401, nsv1052560, nsv1039264, nsv1040584, nsv1046034, nsv1036055, nsv1041405, nsv1046861, nsv1055079, nsv1054477, nsv1044902, nsv1046569, nsv1043351, nsv1055081, nsv1042842, nsv1053761, nsv1050278, nsv1042187, nsv1046096, nsv1043130, nsv1040963, nsv1046131, nsv1049023, nsv1042358, nsv1049827, nsv1043747, nsv1040550, nsv1038765, nsv1053219, nsv1035244, nsv1041867, nsv1046461, nsv1037212, nsv1038293, nsv1044754, nsv1038061, nsv1054329, nsv1050030, nsv1049899, nsv1049656, nsv1047058, nsv1049128, nsv1051428, nsv1052077, nsv1038337, nsv1048564, nsv1046702, nsv1050963, nsv1053551, nsv1043733, nsv1054463, nsv1051146, nsv1043124, nsv1039147, nsv1038983, nsv1052599, nsv1038940, nsv1042326, nsv1053301, nsv1037441, nsv1047119, nsv1042706, nsv1053233, nsv1035962, nsv1041115, nsv1047541, nsv1054967, nsv1039795, nsv1047123, nsv1039257, nsv1048400, nsv1048572, nsv1046834, nsv1038959, nsv1047402, nsv1040818, nsv1039727, nsv1043257, nsv1055129, nsv1054314, nsv1035177, nsv1054009, nsv1044724, nsv1038732, nsv1038883, nsv1037945, nsv1046290, nsv1049815, nsv1054924, nsv1038861, nsv1039782, nsv1053210, nsv1038869, nsv1048986, nsv1041590, nsv1046215
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2238n100
Frequency
Sample Size11257
Observed Gain125
Observed Loss0
Observed Complex0
Frequencyn/a


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