A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2563n100



Internal ID19012931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34421910..34585552hg38UCSC Ensembl
chr15:34714111..34877753hg19UCSC Ensembl
chr15:32501403..32665045hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38163643
hg19163643
hg18163643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045068, nsv1038804, nsv1039342, nsv1044586, nsv1046979, nsv1051213, nsv1048580, nsv1035639, nsv1048956, nsv1053800, nsv1049914, nsv1040470, nsv1041232, nsv1043642, nsv1040243, nsv1053795, nsv1050147, nsv1040772, nsv1042456, nsv1046335, nsv1041114, nsv1047637, nsv1038550, nsv1045531, nsv1053703, nsv1039545, nsv1053349, nsv1043665, nsv1041494, nsv1046704, nsv1054359, nsv1041760, nsv1037332, nsv1054994, nsv1053356, nsv1046848
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2563n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss201
Observed Complex0
Frequencyn/a


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