A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3308779



Internal ID15155728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37415661..37415662hg38UCSC Ensembl
Innerchr15:37415611..37415712hg38UCSC Ensembl
Outerchr15:37415610..37415713hg38UCSC Ensembl
chr15:37707862..37707863hg19UCSC Ensembl
Innerchr15:37707812..37707913hg19UCSC Ensembl
Outerchr15:37707811..37707914hg19UCSC Ensembl
chr15:35495154..35495155hg18UCSC Ensembl
Innerchr15:35495205..35495104hg18UCSC Ensembl
Outerchr15:35495103..35495206hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38661
hg19661
hg18661
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7836981
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3308779
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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