A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3430887



Internal ID14931157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77485980..77485980hg38UCSC Ensembl
Innerchr9:77485979..77485981hg38UCSC Ensembl
Outerchr9:77485930..77486030hg38UCSC Ensembl
chr9:80100896..80100896hg19UCSC Ensembl
Innerchr9:80100895..80100897hg19UCSC Ensembl
Outerchr9:80100846..80100946hg19UCSC Ensembl
chr9:79290716..79290716hg18UCSC Ensembl
Innerchr9:79290717..79290715hg18UCSC Ensembl
Outerchr9:79290666..79290766hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38746
hg19746
hg18746
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8741369
SamplesNA19240
Known GenesGNA14
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3430887
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