A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1050n145



Internal ID22814066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78810928..78814066hg38UCSC Ensembl
chr6:79520645..79523783hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg383139
hg193139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114871, nsv3117934, nsv3111929, nsv3118054
Samplessample379, sample38, sample396, sample313, sample262, sample184, sample203, sample221, sample80, sample266, sample423, sample50, sample173, sample171, sample325, sample232, sample28, sample211, sample186, sample206, sample178, sample390, sample169, sample120, sample176, sample403, sample32, sample153, sample407, sample25, sample118, sample304, sample194, sample233, sample302, sample47, sample212, sample368, sample97, sample391, sample1, sample335, sample89, sample35, sample155, sample292, sample113
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1050n145
Frequency
Sample Size467
Observed Gain0
Observed Loss47
Observed Complex0
Frequencyn/a


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