A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv469e59



Internal ID20127218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86524708..86524819hg38UCSC Ensembl
chr10:88284465..88284576hg19UCSC Ensembl
chr10:88274445..88274556hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38112
hg19112
hg18112
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3302874, esv3302624
SamplesNA18502, NA18947, NA18861, NA18508, NA10851, NA12414, NA18507, NA11920, NA11931, NA18870, NA18550, NA12891, NA18916, NA12287, NA19138, NA19137, NA19238, NA12878, NA11894, NA12892, NA19225, NA18858, NA18945, NA19108, NA18517, NA19240, NA07037, NA18501, NA19093, NA18505, NA12006, NA18511, NA12776, NA18965
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv469e59
Frequency
Sample Size185
Observed Gain34
Observed Loss0
Observed Complex0
Frequencyn/a


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