A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv117e199



Internal ID22757890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8023953..8025355hg38UCSC Ensembl
chr10:8065916..8067318hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381403
hg191403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658404, esv2676545
SamplesNA18502, NA19701, HG00442, NA19058, NA18924, HG01462, HG00608, NA19909, NA11829, NA19399, NA19914, NA19704, NA18917, NA19350, NA19777, NA20332, NA20346, NA19443, NA19190, NA12400, NA18988, NA18571, NA18977, NA18868, NA20340, NA19371, NA19235, NA19471, HG00705, NA18986, NA19087, NA19002, NA19901, NA19985, HG00264, NA20818, NA19908, NA19056, NA18933, HG00533, NA18579, NA18871, NA20344, NA11919, NA19084, HG00404, NA11893, NA18853, NA19452, HG00463, NA19160, HG00246, NA19003, NA19440, NA18533, NA19321, NA19473, NA19380, HG01357, NA19818, HG00578, NA19474, NA18873, NA19780, NA19213, NA19900, HG01378, NA18488, HG01111, HG01082, NA19312, HG01125, NA18623, NA18522, NA19429, NA12776, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv117e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss77
Observed Complex0
Frequencyn/a


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