A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1815e59



Internal ID18987316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74727418..74729416hg38UCSC Ensembl
chr17:72723557..72725555hg19UCSC Ensembl
chr17:70235152..70237150hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381999
hg191999
hg181999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3446039, esv3360135, esv3346821
SamplesNA19239, NA19238, NA19240
Known GenesRAB37
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1815e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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