A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv221e199



Internal ID22757994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67707185..67987103hg38UCSC Ensembl
chr11:67474656..67754574hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38279919
hg19279919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2667988, esv2678476
SamplesHG00113, HG00258, NA18542, NA07051
Known GenesFAM86C2P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv221e199
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