A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2959e59



Internal ID22764179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35772671..35772786hg38UCSC Ensembl
chr4:35774293..35774408hg19UCSC Ensembl
chr4:35450688..35450803hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38116
hg19116
hg18116
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3302543, esv3303016
SamplesNA12004, NA18504, NA19138, NA19238, NA18858, NA18909, NA19147, NA19240, NA18501
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2959e59
Frequency
Sample Size185
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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