A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659172



Internal ID9925277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55654858..55836170hg38UCSC Ensembl
chr11:55422334..55603646hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38181313
hg19181313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv212e199
Supporting Variantsessv5969465, essv6561943, essv6322775, essv5433376, essv5802280
SamplesNA19347, NA19435, HG01375, NA19376, NA19093
Known GenesOR4C6, OR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659172
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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