A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664207



Internal ID9930312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103310059..103311250hg38UCSC Ensembl
chr10:105069816..105071007hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg381192
hg191192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6547043, essv5839818, essv5994575, essv5462180
SamplesNA19443, NA19440, NA19428, NA19474
Known GenesPCGF6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664207
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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