A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3305879



Internal ID15152827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51891709..51891710hg38UCSC Ensembl
Innerchr15:51891678..51891741hg38UCSC Ensembl
Outerchr15:51891677..51891742hg38UCSC Ensembl
chr15:52183906..52183907hg19UCSC Ensembl
Innerchr15:52183875..52183938hg19UCSC Ensembl
Outerchr15:52183874..52183939hg19UCSC Ensembl
chr15:49971198..49971199hg18UCSC Ensembl
Innerchr15:49971230..49971167hg18UCSC Ensembl
Outerchr15:49971166..49971231hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38215
hg19215
hg18215
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7748206, essv7760969, essv7743602, essv7750902, essv7762605, essv7757226
SamplesNA11920, NA18558, NA18579, NA18948, NA18961, NA18609
Known GenesTMOD3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3305879
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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