A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3310307



Internal ID15157258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38047038..38047039hg38UCSC Ensembl
Innerchr15:38047009..38047068hg38UCSC Ensembl
Outerchr15:38047008..38047069hg38UCSC Ensembl
chr15:38339239..38339240hg19UCSC Ensembl
Innerchr15:38339210..38339269hg19UCSC Ensembl
Outerchr15:38339209..38339270hg19UCSC Ensembl
chr15:36126531..36126532hg18UCSC Ensembl
Innerchr15:36126561..36126502hg18UCSC Ensembl
Outerchr15:36126501..36126562hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38211
hg19211
hg18211
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7838549
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3310307
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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