A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660510



Internal ID9926615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5375597..5378268hg38UCSC Ensembl
chr5:5375710..5378381hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg382672
hg192672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5940954, essv5874193
SamplesNA20787, NA12778
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660510
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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