A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3304017



Internal ID15150965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111465192..111465193hg38UCSC Ensembl
Innerchr1:111465153..111465232hg38UCSC Ensembl
Outerchr1:111465152..111465233hg38UCSC Ensembl
chr1:112007814..112007815hg19UCSC Ensembl
Innerchr1:112007775..112007854hg19UCSC Ensembl
Outerchr1:112007774..112007855hg19UCSC Ensembl
chr1:111809337..111809338hg18UCSC Ensembl
Innerchr1:111809377..111809298hg18UCSC Ensembl
Outerchr1:111809297..111809378hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38632
hg19632
hg18632
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7752656
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3304017
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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