A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1171n145



Internal ID22814187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39368796..39530975hg38UCSC Ensembl
chr8:39226315..39388494hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38162180
hg19162180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117717, nsv3112436, nsv3114488, nsv3116328, nsv3117147
Samplessample379, sample133, sample373, sample203, sample115, sample316, sample382, sample159, sample346, sample182, sample266, sample222, sample330, sample365, sample170, sample329, sample9, sample402, sample87, sample82, sample404, sample232, sample358, sample202, sample348, sample190, sample143, sample363, sample291, sample71, sample206, sample59, sample216, sample31, sample195, sample345, sample392, sample270, sample151, sample416, sample235, sample153, sample300, sample375, sample56, sample424, sample54, sample299, sample25, sample55, sample339, sample395, sample290, sample276, sample191, sample385, sample418, sample233, sample137, sample102, sample227, sample296, sample148, sample253, sample68, sample192, sample197, sample117, sample47, sample368, sample97, sample278, sample391, sample107, sample250, sample275, sample155, sample268, sample163, sample110, sample150
Known GenesADAM3A, ADAM5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1171n145
Frequency
Sample Size467
Observed Gain0
Observed Loss81
Observed Complex0
Frequencyn/a


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