A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7752656



Internal ID15138526
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 StatusS
Merged Variantsesv3304017
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7752656
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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