A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv379e199



Internal ID20123681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108294097..108300744hg38UCSC Ensembl
chr13:108946445..108953092hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg386648
hg196648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2675603, esv2658884, esv2678008
SamplesHG00096, NA20588, NA11830, NA20529, HG01356, HG00143, HG00142, NA20508, NA19664, NA11995, HG00242, NA18508, NA12273, NA19332, NA11920, NA11933, NA18599, NA12045, HG00367, HG00318, NA19350, NA19092, HG00153, NA20294, NA19819, NA19393, NA18504, NA12340, HG01456, HG01461, NA19443, NA19098, NA12400, NA20806, HG01140, NA12341, HG00271, NA12813, HG00127, NA19660, NA19379, NA18550, NA18519, HG00251, NA18489, HG01177, NA18923, NA11992, NA19197, NA18582, NA12283, HG01354, HG00369, HG01365, HG00185, NA20336, NA19904, NA19384, HG01110, NA19130, HG00158, HG00139, NA20539, NA19651, HG00120, NA18874, HG00106, HG00156, NA19917, NA19719, NA12044, NA11994, NA19235, NA19471, NA19159, HG00309, HG00338, NA19239, NA20342, NA19209, HG00178, NA20757, NA18908, NA19451, HG00264, NA11993, HG00108, HG00133, HG01136, HG00154, NA19908, NA20800, HG00282, NA18934, HG00557, HG00245, NA19462, NA19152, HG00190, NA20760, NA20536, NA19327, NA19455, NA20314, NA19982, HG00320, NA18637, NA12718, NA18871, NA18534, NA20770, HG01047, HG00273, NA19114, HG00651, NA19774, HG00250, HG00531, NA11893, NA20538, NA12249, NA19453, NA06989, NA18553, NA19338, HG00146, NA19452, HG00141, NA19469, NA19395, HG00126, NA19436, NA19401, NA19375, NA20799, HG00124, HG00155, NA19440, NA12716, HG00254, NA19390, NA19108, NA19147, NA18517, NA12775, NA19749, NA20815, HG00357, NA19732, HG00136, NA19435, NA20530, NA19835, NA20792, NA19439, NA19467, HG01108, NA07037, HG00256, NA19783, NA06986, HG00269, HG00125, NA20341, NA19818, NA19376, HG00707, HG00111, NA19248, HG01491, NA20582, NA19779, NA19716, HG00174, HG00123, NA20289, HG00186, NA18873, NA19213, HG00372, HG00252, NA20503, NA20502, NA19430, NA07056, NA11892, HG01378, NA19755, NA19316, NA20585, NA19065, NA18549, NA18487, NA19153, NA12776
Known GenesTNFSF13B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv379e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss195
Observed Complex0
Frequencyn/a


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