A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3309611



Internal ID15156562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39289615..39289616hg38UCSC Ensembl
Innerchr3:39289599..39289632hg38UCSC Ensembl
Outerchr3:39289598..39289633hg38UCSC Ensembl
chr3:39331106..39331107hg19UCSC Ensembl
Innerchr3:39331090..39331123hg19UCSC Ensembl
Outerchr3:39331089..39331124hg19UCSC Ensembl
chr3:39306110..39306111hg18UCSC Ensembl
Innerchr3:39306127..39306094hg18UCSC Ensembl
Outerchr3:39306093..39306128hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38156
hg19156
hg18156
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7843150, essv7842174
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3309611
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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