A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1376e199



Internal ID20124678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127419166..127424813hg38UCSC Ensembl
chr9:130181445..130187092hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385648
hg195648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2667187, esv2662140
SamplesNA20761, HG00650, HG01173, HG00143, HG00608, NA19909, NA20508, NA19664, HG00242, HG00559, NA18565, NA12843, NA20752, NA18999, NA19684, NA18530, NA18959, NA18616, HG01461, NA18563, HG00641, HG00138, HG01350, NA18567, NA18960, HG01365, HG00537, NA18949, HG00512, NA12275, NA19720, HG01080, NA20518, NA20812, HG00325, NA11932, HG00534, HG00705, NA19722, NA18990, HG01198, NA18557, HG01048, HG01133, HG00326, NA20757, NA18539, NA19921, NA20753, HG01124, NA18538, NA19056, NA19670, HG00557, HG00657, NA20810, NA20314, NA19663, NA19081, HG01498, HG00275, NA12718, NA20519, NA18572, NA18948, NA18534, NA18981, NA18548, NA18537, NA19654, HG00250, NA19084, HG00690, HG00531, HG00331, NA18553, HG01497, NA19761, HG00146, NA12144, NA18570, HG00126, NA18593, NA12546, NA18541, NA18974, NA19729, HG00611, NA19652, HG00336, HG00625, NA18564, NA19072, HG00580, HG00734, NA20527, HG01375, NA20792, NA20778, NA19679, HG01137, NA18943, NA19783, HG00662, NA18615, HG01489, HG01342, HG00620, NA19785, HG00259, NA19779, NA20510, NA18609, NA19780, NA18983, HG00274, NA18989, NA11892, HG00171, NA12890, NA19074, HG00581, NA18620, HG00626, HG00114, HG01441, NA19648, HG00536, NA11995, HG01359, NA18980, NA18561, NA19704, HG01389, HG01374, HG00306, NA19092, HG01465, NA19057, NA18596, HG00566, NA18526, NA12155, HG01140, NA12341, NA20537, HG01250, NA19746, NA19076, NA19005, HG01366, HG00501, NA19762, NA18595, HG01488, HG00702, NA19723, NA18982, NA18635, NA18619, NA20769, NA12348, HG00634, NA18942, NA12283, NA19771, NA19088, NA19054, HG00369, HG00270, NA19782, NA19681, HG01110, HG00590, NA18611, NA12761, HG01455, NA06984, HG00236, HG01495, HG00262, NA19719, NA18560, NA19731, NA19075, NA18617, HG01176, HG01440, NA19002, HG00637, HG00530, HG01136, NA18544, HG00560, NA18613, NA19657, NA19707, NA19077, HG00701, HG01515, HG00436, NA19788, NA18976, NA20770, HG00708, HG00635, NA18566, NA19774, NA19000, NA19655, NA18856, HG01383, HG00525, NA19756, NA19160, NA18634, HG01204, NA18576, NA18546, HG00124, NA20522, NA18542, NA20801, NA12716, HG01190, NA18559, HG00565, NA18950, NA19732, HG01253, NA20804, NA19773, NA19786, HG00125, NA19759, HG00578, HG01491, NA19060, NA18987, HG00656, HG01055, NA12830, NA19726, NA18552, HG01251, NA19661, NA18984, NA19755, NA19004, NA19758, HG00554, NA18549
Known GenesZNF79
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1376e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss252
Observed Complex0
Frequencyn/a


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