A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3429438



Internal ID14929708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8327114..8332508hg38UCSC Ensembl
Innerchr9:8329104..8330928hg38UCSC Ensembl
Outerchr9:8327004..8332628hg38UCSC Ensembl
chr9:8327114..8332508hg19UCSC Ensembl
Innerchr9:8329104..8330928hg19UCSC Ensembl
Outerchr9:8327004..8332628hg19UCSC Ensembl
chr9:8317114..8322508hg18UCSC Ensembl
Innerchr9:8319104..8320928hg18UCSC Ensembl
Outerchr9:8317004..8322628hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg385395
hg195395
hg185395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8809590
SamplesNA12878
Known GenesPTPRD
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3429438
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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