A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4371e59



Internal ID22765591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62357255..62365753hg38UCSC Ensembl
chr9:46668556..46677054hg19UCSC Ensembl
chr9:46508552..46517050hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388499
hg198499
hg188499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3334124, esv3367554
SamplesNA12878, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4371e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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