A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3365040



Internal ID14865300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26000299..26002367hg38UCSC Ensembl
Innerchr21:26000787..26002289hg38UCSC Ensembl
Outerchr21:26000189..26002487hg38UCSC Ensembl
chr21:27372614..27374682hg19UCSC Ensembl
Innerchr21:27373102..27374604hg19UCSC Ensembl
Outerchr21:27372504..27374802hg19UCSC Ensembl
chr21:26294485..26296553hg18UCSC Ensembl
Innerchr21:26296475..26294973hg18UCSC Ensembl
Outerchr21:26294375..26296673hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg382069
hg192069
hg182069
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8809018
SamplesNA12878
Known GenesAPP
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3365040
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