A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666790



Internal ID9932895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133509669..133535535hg38UCSC Ensembl
Outerchr4:133509632..133535585hg38UCSC Ensembl
Innerchr4:134430824..134456690hg19UCSC Ensembl
Outerchr4:134430787..134456740hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3825954
hg1925954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6484655
SamplesHG00251
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666790
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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