A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3366706



Internal ID15213683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15920531..15921929hg38UCSC Ensembl
Innerchr4:15920929..15921531hg38UCSC Ensembl
Outerchr4:15919531..15922929hg38UCSC Ensembl
chr4:15922154..15923552hg19UCSC Ensembl
Innerchr4:15922552..15923154hg19UCSC Ensembl
Outerchr4:15921154..15924552hg19UCSC Ensembl
chr4:15531252..15532650hg18UCSC Ensembl
Innerchr4:15532252..15531650hg18UCSC Ensembl
Outerchr4:15530252..15533650hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8694259
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3366706
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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