A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2923e59



Internal ID20129672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5855724..5857722hg38UCSC Ensembl
chr4:5857451..5859449hg19UCSC Ensembl
chr4:5908352..5910350hg18UCSC Ensembl
Cytoband4p16.1
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 Variantsesv3350523, esv3430862, esv3401007
SamplesNA19239, NA19238, NA19240
Known GenesCRMP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2923e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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