A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3353687



Internal ID15200668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3803886..3803886hg38UCSC Ensembl
Innerchr11:3803885..3803887hg38UCSC Ensembl
Outerchr11:3803836..3803936hg38UCSC Ensembl
chr11:3825116..3825116hg19UCSC Ensembl
Innerchr11:3825115..3825117hg19UCSC Ensembl
Outerchr11:3825066..3825166hg19UCSC Ensembl
chr11:3781692..3781692hg18UCSC Ensembl
Innerchr11:3781693..3781691hg18UCSC Ensembl
Outerchr11:3781642..3781742hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38652
hg19652
hg18652
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8740724
SamplesNA19240
Known GenesPGAP2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3353687
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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