A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3329848



Internal ID15176834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11373456..11374474hg38UCSC Ensembl
Innerchr1:11373456..11374474hg38UCSC Ensembl
Outerchr1:11373270..11375061hg38UCSC Ensembl
chr1:11433513..11434531hg19UCSC Ensembl
Innerchr1:11433513..11434531hg19UCSC Ensembl
Outerchr1:11433327..11435118hg19UCSC Ensembl
chr1:11356100..11357118hg18UCSC Ensembl
Innerchr1:11356100..11357118hg18UCSC Ensembl
Outerchr1:11355914..11357705hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381019
hg191019
hg181019
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8652037
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3329848
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