A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7750563



Internal ID15122963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120158756..120158757hg38UCSC Ensembl
Innerchr9:120158699..120158814hg38UCSC Ensembl
Outerchr9:120158698..120158815hg38UCSC Ensembl
chr9:122921034..122921035hg19UCSC Ensembl
Innerchr9:122920977..122921092hg19UCSC Ensembl
Outerchr9:122920976..122921093hg19UCSC Ensembl
chr9:121960855..121960856hg18UCSC Ensembl
Innerchr9:121960913..121960798hg18UCSC Ensembl
Outerchr9:121960797..121960914hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38219
hg19219
hg18219
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3306653
Supporting Variants
SamplesNA19257
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7750563
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