A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv736e59



Internal ID22761956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45001..60823hg38UCSC Ensembl
chr12:151291..169989hg19UCSC Ensembl
chr12:21552..40250hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3815823
hg1918699
hg1818699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3428761, esv3416988
SamplesNA19238, NA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv736e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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