A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3309407



Internal ID15156357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36009086..36009087hg38UCSC Ensembl
Innerchr1:36009060..36009113hg38UCSC Ensembl
Outerchr1:36009059..36009114hg38UCSC Ensembl
chr1:36474687..36474688hg19UCSC Ensembl
Innerchr1:36474661..36474714hg19UCSC Ensembl
Outerchr1:36474660..36474715hg19UCSC Ensembl
chr1:36247274..36247275hg18UCSC Ensembl
Innerchr1:36247301..36247248hg18UCSC Ensembl
Outerchr1:36247247..36247302hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38133
hg19133
hg18133
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7837169
SamplesNA19239
Known GenesAGO3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3309407
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer