A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3303021



Internal ID15149969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15945362..15947344hg38UCSC Ensembl
Innerchr4:15945462..15947244hg38UCSC Ensembl
Outerchr4:15945262..15947444hg38UCSC Ensembl
chr4:15946985..15948967hg19UCSC Ensembl
Innerchr4:15947085..15948867hg19UCSC Ensembl
Outerchr4:15946885..15949067hg19UCSC Ensembl
chr4:15556083..15558065hg18UCSC Ensembl
Innerchr4:15556183..15557965hg18UCSC Ensembl
Outerchr4:15555983..15558165hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg381983
hg191983
hg181983
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7732784, essv7739107
SamplesNA18916, NA19099
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3303021
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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