A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1037e199



Internal ID20124339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110124239..110143707hg38UCSC Ensembl
chr5:109459940..109479408hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3819469
hg1919469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2659296, esv2678715
SamplesNA19701, NA19703, NA19399, NA19704, NA19350, NA19359, NA19092, NA19819, NA19393, NA20346, NA19443, NA20356, NA19920, NA19446, HG00641, NA18519, NA19382, NA19315, NA19448, NA19916, NA19457, NA19313, NA19138, NA19904, NA19384, NA20291, NA19404, NA19383, NA18868, NA19235, NA19385, NA19471, NA19317, NA19901, NA18520, NA19456, NA19445, NA19985, NA18867, NA19908, NA19347, NA19391, NA19327, NA18871, NA18907, HG01073, NA19449, NA19453, NA18853, NA19338, NA19469, NA19318, NA19375, NA19834, NA19321, NA20276, NA19434, NA19473, NA19435, NA19444, NA19331, HG01174, NA19470, NA19428, NA19467, NA19360, NA19398, NA19328, NA20348, NA19248, NA19438, NA19472, NA19468, NA19713, NA19474, NA19102, NA18873, NA19711, NA19213, NA19316, NA19312, NA18487
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1037e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss82
Observed Complex0
Frequencyn/a


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