A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv71e59



Internal ID22761291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25508774..25509072hg38UCSC Ensembl
chr1:25835265..25835563hg19UCSC Ensembl
chr1:25707852..25708150hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38299
hg19299
hg18299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3445747, esv3413689
SamplesNA12891, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv71e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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