A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2960e59



Internal ID22764180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37330735..37331633hg38UCSC Ensembl
chr4:37332357..37333255hg19UCSC Ensembl
chr4:37008752..37009650hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3387232, esv3413175, esv3323990
SamplesNA19238, NA19239, NA19240
Known GenesKIAA1239
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2960e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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