A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667023



Internal ID9933128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5763343..5788052hg38UCSC Ensembl
chr11:5784573..5809282hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824710
hg1924710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv189e199
Supporting Variantsessv6056420, essv6210498, essv6318636, essv6220671, essv5825601, essv6222459, essv5523524, essv5884329, essv5416411, essv5695497, essv6543135, essv6134471, essv5551788
SamplesNA11995, NA10851, NA18507, NA11931, NA18940, NA19239, NA11993, NA18951, NA19225, NA12144, NA18501, NA12749, NA18511
Known GenesOR52N1, OR52N5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667023
Frequency
Sample Size1151
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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