A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307817



Internal ID15154765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34824558..34824559hg38UCSC Ensembl
Innerchr9:34824539..34824578hg38UCSC Ensembl
Outerchr9:34824538..34824579hg38UCSC Ensembl
chr9:34824555..34824556hg19UCSC Ensembl
Innerchr9:34824536..34824575hg19UCSC Ensembl
Outerchr9:34824535..34824576hg19UCSC Ensembl
chr9:34814555..34814556hg18UCSC Ensembl
Innerchr9:34814575..34814536hg18UCSC Ensembl
Outerchr9:34814535..34814576hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38102
hg19102
hg18102
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7802774, essv7782480, essv7833634, essv7788786
SamplesNA12814, NA12873, NA07037, NA06986
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307817
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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