A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3402887



Internal ID15249849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90777890..90777899hg38UCSC Ensembl
Innerchr9:90777871..90777918hg38UCSC Ensembl
Outerchr9:90777862..90777927hg38UCSC Ensembl
chr9:93540172..93540181hg19UCSC Ensembl
Innerchr9:93540153..93540200hg19UCSC Ensembl
Outerchr9:93540144..93540209hg19UCSC Ensembl
chr9:92579993..92580002hg18UCSC Ensembl
Innerchr9:92580021..92579974hg18UCSC Ensembl
Outerchr9:92579965..92580030hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7864947
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3402887
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