A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2962n100



Internal ID22789049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:35207424..35550220hg38UCSC Ensembl
chr16:34441795..34784591hg19UCSC Ensembl
chr16:34299296..34642092hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38342797
hg19342797
hg18342797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057261, nsv1067024, nsv1057446, nsv1055757, nsv1057724, nsv1056878, nsv1059193, nsv1058121, nsv1055143, nsv1059623, nsv1060070, nsv1062966, nsv1065697, nsv1061797, nsv1058910, nsv1064185, nsv1055333, nsv1059662, nsv1058266, nsv1055579, nsv1059628, nsv1061874, nsv1057293, nsv1064337, nsv1063070, nsv1061702, nsv1063520, nsv1066561, nsv1057399, nsv1058634, nsv1062708, nsv1061290, nsv1062987, nsv1057401, nsv1056820, nsv1056720, nsv1061459, nsv1064921, nsv1061194, nsv1063303, nsv1061997, nsv1064513, nsv1062345, nsv1066582, nsv1065916, nsv1057773, nsv1055662, nsv1065341, nsv1057559, nsv1055529, nsv1058377, nsv1060964, nsv1057372, nsv1060407, nsv1056523, nsv1066781, nsv1057707, nsv1066133, nsv1058917, nsv1055219, nsv1058284, nsv1066957, nsv1062346, nsv1056693, nsv1065700, nsv1061680, nsv1062053, nsv1059371, nsv1064778, nsv1061166, nsv1064015, nsv1065682, nsv1064887, nsv1058807, nsv1057095, nsv1059458, nsv1062190, nsv1063364, nsv1055478, nsv1064828, nsv1058754, nsv1066148, nsv1063057, nsv1065125, nsv1064567, nsv1063447, nsv1058916, nsv1056156, nsv1056289, nsv1058771, nsv1065747, nsv1058753, nsv1057967, nsv1056269, nsv1063304, nsv1062138, nsv1067213, nsv1060680, nsv1066668, nsv1058912, nsv1065420, nsv1062136, nsv1058461, nsv1065413, nsv1065949, nsv1059510, nsv1066465, nsv1056518, nsv1062054, nsv1061787, nsv1059760, nsv1060000, nsv1059806, nsv1064672, nsv1063796, nsv1059736, nsv1066157, nsv1057427, nsv1066102, nsv1059323, nsv1056346, nsv1058997, nsv1056564, nsv1056265, nsv1055980, nsv1062355, nsv1062022, nsv1064573, nsv1063379, nsv1066450, nsv1065085, nsv1056379, nsv1061808, nsv1063214, nsv1065278
Samples
Known GenesLOC100130700, LOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2962n100
Frequency
Sample Size11257
Observed Gain1614
Observed Loss0
Observed Complex0
Frequencyn/a


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