A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3147n100



Internal ID20154763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36102943..36215877hg38UCSC Ensembl
chr17:34430336..34543331hg19UCSC Ensembl
chr17:31454449..31567444hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38112935
hg19112996
hg18112996
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066309, nsv1061969, nsv1059528, nsv1063002, nsv1067285, nsv1063428, nsv1064028, nsv1058889, nsv1067508, nsv1059073, nsv1065861, nsv1060707, nsv1060217, nsv1066196
Samples
Known GenesCCL3L1, CCL3L3, CCL4, CCL4L1, CCL4L2, TBC1D3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3147n100
Frequency
Sample Size29084
Observed Gain184
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer