A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659086



Internal ID9578505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:991183..997744hg38UCSC Ensembl
Outerchr3:991026..997897hg38UCSC Ensembl
Innerchr3:1032867..1039428hg19UCSC Ensembl
Outerchr3:1032710..1039581hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg386872
hg196872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5570466, essv5468599, essv5508049, essv5968575, essv6247099
SamplesNA19107, NA18907, NA18909, NA18501, NA18522
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659086
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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