A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1760e59



Internal ID20128509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45511903..45520201hg38UCSC Ensembl
chr17:43589269..43597567hg19UCSC Ensembl
chr17:40945052..40953350hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg388299
hg198299
hg188299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3425595, esv3375825, esv3428679, esv3367367, esv3378464, esv3402129
SamplesNA12891, NA19238, NA19239, NA12878, NA12892, NA19240
Known GenesLRRC37A4P
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1760e59
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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