A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660659



Internal ID9926764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39702889..39712160hg38UCSC Ensembl
Outerchr4:39702732..39712313hg38UCSC Ensembl
Innerchr4:39704509..39713780hg19UCSC Ensembl
Outerchr4:39704352..39713933hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg389582
hg199582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5994714, essv6026475, essv6395723, essv6321132, essv5588039, essv6347089
SamplesHG00122, HG00137, HG00273, HG00126, HG00136, HG00116
Known GenesUBE2K
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660659
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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