A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv741e59



Internal ID20127490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3197825..3199023hg38UCSC Ensembl
chr12:3306991..3308189hg19UCSC Ensembl
chr12:3177252..3178450hg18UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3390004, esv3341650
SamplesNA19239, NA19240
Known GenesTSPAN9
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv741e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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