A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1076e199



Internal ID22758849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17376461..17381361hg38UCSC Ensembl
chr6:17376692..17381592hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384901
hg194901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2666977, esv2672815
SamplesHG00096, NA19394, HG00542, NA19648, HG00143, NA19703, NA19332, HG00100, HG01188, HG00151, NA20813, HG01465, NA19819, NA20808, HG00177, HG00654, HG01051, HG01140, HG00327, NA20814, HG00138, NA19373, NA19076, HG01070, HG00251, HG00122, NA18597, HG00173, NA19723, HG00736, NA07048, HG00346, NA19313, HG00247, NA19054, HG00243, NA19079, HG00590, HG00158, HG00139, NA12275, HG00120, NA19383, HG00106, HG01170, NA20812, HG00232, NA19731, HG00705, HG01440, HG00309, HG00118, HG01133, HG00326, HG00178, NA20127, HG00323, HG00253, NA19921, HG01124, HG00313, HG00137, HG01136, HG00188, HG00149, NA18605, HG00731, HG00176, NA19707, NA19403, HG00557, NA12342, HG00732, HG00275, NA12718, NA18572, HG01149, NA19776, HG00708, HG00692, NA19064, HG01390, HG00324, NA11919, NA20299, NA20581, HG00331, HG00684, HG01383, HG01101, NA19059, NA19761, HG00152, NA18523, HG00463, NA12778, HG00126, HG01075, HG00124, NA19652, HG00265, HG00565, HG00366, NA20815, HG00357, HG00278, NA07051, HG01375, NA19786, HG00319, HG00116, NA19083, HG01108, NA07037, NA19376, NA19716, NA19474, HG01055, HG00280, NA19116, HG01251, NA20503, HG01377, NA19312, HG00171, NA20322, NA18623, NA20585, NA19065, HG01191, NA18487, HG01437, HG01061, HG00553, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1076e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss135
Observed Complex0
Frequencyn/a


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