A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3532e59



Internal ID18989033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57924315..57927113hg38UCSC Ensembl
chr6:58250593..58253391hg19UCSC Ensembl
chr6:58358552..58361350hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg382799
hg192799
hg182799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3411255, esv3445668
SamplesNA19239, NA19240
Known GenesGUSBP4
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3532e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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