A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676819



Internal ID9596238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55598440..55696946hg38UCSC Ensembl
Outerchr11:55598069..55697316hg38UCSC Ensembl
Innerchr11:55365916..55464422hg19UCSC Ensembl
Outerchr11:55365545..55464792hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3899248
hg1999248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv211e199
Supporting Variantsessv6145732, essv6435598, essv6582299, essv6234467, essv5564068, essv5937639, essv6409453, essv5694281, essv5764570, essv5876839, essv6333454, essv5752251, essv6420162, essv6494665, essv6522479, essv6153130, essv6423595, essv6190056, essv6379764, essv5519811, essv5774380, essv6525634, essv6270462, essv5761593, essv5653314, essv5503399, essv6209327, essv5856976, essv6566283, essv6340950, essv6132002, essv6156289, essv5715476, essv6121673, essv6464270, essv5840240, essv5881353, essv5550314, essv5846141, essv6076870, essv5632067
SamplesNA12383, NA11829, NA12414, NA12843, NA11920, NA12340, NA12058, NA12750, NA12399, NA07357, NA12341, NA07346, NA12348, NA11992, NA07048, NA11918, NA07347, NA12761, NA11930, NA12282, NA12275, NA06984, NA12828, NA12748, NA11831, NA10847, NA12342, NA12003, NA11894, NA06989, NA12827, NA12043, NA11881, NA12775, NA12046, NA12763, NA12347, NA06994, NA12006, NA12776, NA11832
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676819
Frequency
Sample Size1151
Observed Gain0
Observed Loss41
Observed Complex0
Frequencyn/a


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