A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv73e199



Internal ID20123375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158757135..158758219hg38UCSC Ensembl
chr1:158726925..158728009hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381085
hg191085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2661235, esv2675661
SamplesHG00626, NA18502, HG00542, NA19058, NA20543, HG00536, HG00231, HG00608, NA19909, NA12286, NA11995, NA11829, HG00671, HG00361, NA10851, NA19704, NA18507, HG01389, NA18999, NA18603, NA12045, HG00244, NA18486, NA12004, NA18606, HG00737, NA19190, NA18870, NA18526, NA18602, NA18627, HG00327, HG00663, NA20537, NA07346, NA18563, NA18550, NA18489, NA20589, NA18595, HG00702, HG00689, HG00448, HG01168, NA18635, HG00330, NA19062, NA19138, HG00537, NA18611, NA12275, NA12005, HG01069, HG00120, HG00683, HG00106, NA06984, NA20812, NA20340, NA19238, NA11994, HG00534, HG00422, HG00705, HG00182, HG00427, NA18990, NA18557, NA18867, HG00530, HG00419, HG00253, HG01353, HG00133, HG01183, HG01136, HG00188, HG00154, NA18544, HG00560, HG00443, HG00268, HG00266, HG00183, NA19070, NA19056, HG00596, HG01384, NA12003, HG00428, NA19462, NA20809, HG00653, HG00577, NA20521, HG00701, HG00475, NA19236, HG00556, HG00320, HG00533, HG00344, HG00275, NA18579, NA18534, NA20770, HG00619, HG00635, HG01390, HG01047, NA18566, HG01102, HG00273, NA19114, NA19084, HG00690, HG00373, HG00479, NA20581, NA11894, HG00684, HG01383, HG00117, HG00321, HG00140, NA18853, NA18553, NA12827, NA19099, HG01334, NA19257, NA18555, HG00152, NA18963, HG00704, NA19225, NA20828, NA18523, NA18536, NA12778, HG00246, HG00126, NA18858, NA18634, NA20534, NA18576, NA12043, NA18953, HG00155, NA18909, HG01190, HG00285, NA19834, NA18952, NA19147, HG00357, NA12272, NA20804, NA19240, HG01357, HG01174, HG01375, HG00473, NA20792, HG00237, HG00319, NA20797, NA07037, HG00256, NA12763, HG00662, HG00418, NA18615, NA18610, HG01489, NA12347, HG00125, NA19078, NA18501, HG00672, HG00513, HG00578, HG00259, HG00656, HG01055, NA19093, HG00186, HG00112, HG00698, NA18552, HG00377, NA20503, HG00472, NA18505, NA19129, HG01125, NA18624, NA19463, NA18623, NA18511, NA20509
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv73e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss201
Observed Complex0
Frequencyn/a


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