A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv255n145



Internal ID22813271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42625781..42635919hg38UCSC Ensembl
chr12:43019583..43029721hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3810139
hg1910139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110176, nsv3112895, nsv3114920, nsv3116987
Samplessample425, sample98, sample70, sample133, sample373, sample83, sample366, sample317, sample316, sample11, sample266, sample237, sample370, sample365, sample420, sample9, sample142, sample218, sample82, sample42, sample285, sample208, sample202, sample190, sample95, sample360, sample143, sample128, sample363, sample129, sample41, sample186, sample76, sample178, sample307, sample216, sample213, sample19, sample108, sample345, sample332, sample244, sample416, sample153, sample81, sample111, sample157, sample407, sample424, sample343, sample118, sample339, sample304, sample92, sample79, sample418, sample61, sample233, sample43, sample253, sample175, sample68, sample112, sample245, sample117, sample47, sample331, sample97, sample278, sample21, sample391, sample73, sample318, sample89, sample250, sample172, sample188, sample36, sample113, sample46, sample162, sample110
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv255n145
Frequency
Sample Size467
Observed Gain0
Observed Loss82
Observed Complex0
Frequencyn/a


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