A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1353e199



Internal ID22759126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76940029..76943276hg38UCSC Ensembl
chr9:79554945..79558192hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg383248
hg193248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2659439, esv2674323
SamplesNA20588, NA19394, NA12383, NA19701, NA20761, NA20529, NA19664, HG00242, NA20783, NA20514, NA11920, HG00315, NA20752, NA20512, NA19350, HG00153, NA19355, NA18504, NA20332, NA19377, NA20517, HG01461, NA19443, HG01051, NA19920, HG00261, NA20806, HG01522, HG00337, HG00271, NA07346, HG00641, HG00138, HG01350, HG00272, HG01177, NA19678, HG01492, NA07347, HG01083, HG00334, HG00311, HG00243, HG00158, NA11930, HG00281, NA19720, NA20518, HG00335, HG00148, NA20775, HG01519, NA18868, HG00232, NA12044, NA19722, HG00118, HG01198, NA20342, NA20757, HG00323, HG01550, NA19789, HG01124, HG00137, NA19908, HG00266, HG01171, HG00282, NA20810, NA19455, NA19663, HG00263, HG00275, HG00740, HG01047, HG00324, NA11919, HG00250, NA20581, NA19750, NA06989, HG00140, HG01334, NA19761, NA19682, NA12144, HG00246, NA12546, HG00258, NA19440, HG00254, NA18517, NA20276, NA19712, NA19747, NA20790, HG01375, NA19835, HG00237, NA19470, NA19324, NA19311, HG00116, NA19783, NA12763, HG01342, NA19785, HG00342, NA19716, NA19468, HG00267, NA19093, NA20510, NA20786, HG00280, NA20826, NA20503, NA19430, HG01125, HG00171, NA12154, NA18487, HG01437, HG00553, NA19676, HG01516, HG01441, HG01098, HG00249, NA11995, HG01359, HG01188, NA11933, HG01389, HG01374, NA20813, NA12045, HG00367, HG00318, HG01465, HG00103, NA12004, NA20805, NA19777, NA20808, HG00177, HG00150, NA20507, NA18870, NA12400, NA12413, NA12341, HG00327, NA20537, HG01250, NA19660, NA19201, NA19448, HG01488, HG00173, NA19723, NA19119, NA19916, HG00330, HG00736, NA19649, NA12283, HG01354, NA19771, NA19313, HG00247, HG00270, NA20513, NA19782, NA19681, NA12761, HG01134, HG01455, NA19651, NA06984, HG01170, HG00236, HG01495, NA20340, NA19731, HG01176, NA20811, NA19901, NA19725, NA18520, HG00637, NA19209, HG00178, NA18908, HG00264, NA11993, HG00108, NA20818, HG01183, HG00149, NA19247, NA19657, HG00328, NA12342, NA19347, HG00190, NA20809, HG01515, NA19236, HG00320, HG00533, NA20770, NA20344, NA19776, HG01390, HG01073, HG00273, NA19114, NA19655, HG00373, HG01197, NA18499, NA11894, NA12249, HG01383, HG01182, HG00117, NA12827, HG00276, NA20828, NA19160, NA20542, NA19675, HG01204, NA19436, NA20773, NA20801, HG00119, HG00285, NA19834, HG00375, HG00357, HG00278, HG01494, NA20504, NA19786, HG00319, NA07037, HG00256, NA20582, NA19713, HG01254, HG01055, HG00174, NA19726, HG00343, NA20528, HG00252, NA07056, HG01378, NA20322, NA07000, HG01112, HG00554, HG01191, HG01061, NA19153
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1353e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss268
Observed Complex0
Frequencyn/a


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