A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8809359



Internal ID13651382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145355817..145356267hg38UCSC Ensembl
Innerchr6:145355816..145356268hg38UCSC Ensembl
Outerchr6:145355707..145356387hg38UCSC Ensembl
chr6:145676953..145677403hg19UCSC Ensembl
Innerchr6:145676952..145677404hg19UCSC Ensembl
Outerchr6:145676843..145677523hg19UCSC Ensembl
chr6:145718646..145719096hg18UCSC Ensembl
Innerchr6:145719097..145718645hg18UCSC Ensembl
Outerchr6:145718536..145719216hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38451
hg19451
hg18451
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3334160
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8809359
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