A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv960e59



Internal ID22762180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21153513..21155311hg38UCSC Ensembl
chr13:21727652..21729450hg19UCSC Ensembl
chr13:20625652..20627450hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg381799
hg191799
hg181799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3386378, esv3336873
SamplesNA12891, NA12878
Known GenesSKA3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv960e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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