A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1308n100



Internal ID22787395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134469799..134869379hg38UCSC Ensembl
chr11:134339693..134739273hg19UCSC Ensembl
chr11:133844903..134244483hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38399581
hg19399581
hg18399581
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049470, nsv1053412, nsv1053161, nsv1046541, nsv1054729, nsv1048304, nsv1050736, nsv1051864, nsv1047305, nsv1050261, nsv1042650, nsv1051109, nsv1035475, nsv1047064, nsv1054137, nsv1041620, nsv1050775, nsv1043492, nsv1045340, nsv1040415, nsv1047586, nsv1050160, nsv1041828, nsv1036716, nsv1044117, nsv1046061, nsv1051652, nsv1051453, nsv1050971, nsv1049053, nsv1052748, nsv1053329, nsv1052981
Samples
Known GenesLOC283177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1308n100
Frequency
Sample Size11257
Observed Gain62
Observed Loss0
Observed Complex0
Frequencyn/a


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