A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666171



Internal ID9585590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48963976..49887121hg38UCSC Ensembl
chr11:48985528..49908673hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38923146
hg19923146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6274993
SamplesHG01350
Known GenesFOLH1, LOC440040, TRIM49B, TRIM64C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666171
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