A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv638e199



Internal ID20123940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36348743..36356170hg38UCSC Ensembl
chr19:36839645..36847072hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg387428
hg197428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2660784, esv2658674, esv2664464
SamplesHG01357, NA19248, HG00252, NA18595, NA20771, NA19904, NA18630, HG00418, NA12286, NA19081, NA12342, HG00328, NA19437, HG01083, NA19209, HG00186, HG00131, NA20544, NA20796, NA18526, NA20346, NA19223, NA10847, NA20296, HG00614, HG01365, NA19788, HG01492, NA20800, HG01082, NA20816, NA20529, NA18947, NA19010, HG01174, HG01491, NA18573, NA20778, HG01350, HG00739, NA18541, HG01182, HG00106, HG00701, HG01167, NA20539, HG00683, HG01188, HG00334, NA12776, NA20314, NA19004, HG00557, HG01101, HG01134, HG01168, NA19682, HG00366, NA11893, HG00177, NA18965, NA18488, NA19236, NA20798, HG00319, HG00253, NA18505, NA20521, NA19761, NA19776, NA18596, NA18628, NA19438, NA18868, NA19654, NA20586, HG00247, HG00269, HG00554, HG00592, HG00266, NA19762, NA20532, HG00154, HG01107, HG00339, HG00158, NA11919, NA20533, HG00346, NA18624, HG00179, HG01456, HG00593, NA12282, HG00421, HG01378, NA18635, NA19068, NA19917, NA18536, HG00140, HG00638, NA07357, NA18623, NA19900, NA20504, HG01048, NA20530, NA18617, HG00231, NA20801, HG01047, HG00689, NA18592, NA19083, HG00330, NA07048, NA12761, NA19440, NA20541, HG00150, NA20765, HG00258, HG01360, NA11843, NA19985, NA18976, HG01113, NA18637, NA20282, NA20520, HG00637, NA19681, HG00243, HG00254, NA19663, HG00403, HG01187, NA12777, NA19700, HG00237, NA18539, NA19728, HG01497, NA19055, HG00373, HG00097, NA19247, HG00267, NA19080, HG00124, HG01097, NA07346, NA19172, NA19759, NA19771, NA12892, HG00653, HG00640, HG00732, NA12778, NA12348, NA18498, NA19716, NA20790, NA19102, NA06986, NA20334, HG00176, NA18502, HG00560, NA19713, NA20540, HG01073, NA18977, HG00265, HG00501, NA19901, HG01170, HG00232, HG01176, HG01356, NA18978, HG00478, NA11892, NA18487, NA18564, NA18961, HG00116, HG00277, NA19347, NA20774, NA20828, NA19909, NA20797, HG00513, HG00524, HG01494, NA20542, NA19720, HG00329, NA20766, HG00246, NA19074, NA19159, HG01060, NA18974, NA19777, NA18543, NA18619, NA18987, NA10851, NA20525, NA20581, NA18597, NA19921, NA20756, HG00443, NA18909, HG00181, NA18567, NA19078, HG01334, NA20799, HG00650, NA06984, NA18565, NA19009, HG00138, NA18560, NA18989, NA18971, HG00311, NA18602, NA18577, HG00654, NA12878, HG00530, NA20317, NA19064, HG00123, NA19749, HG00285, NA19063, NA19717, NA12546, HG00142, NA19732, NA19916, NA18610, NA20758, NA12045, NA18984, HG00566, NA19756, NA19171, HG00119, HG00275, HG00641, NA18853, NA20524, NA20804, NA20806, NA06994, NA18615, NA20502, NA19087, NA18555, NA19385, HG00278, NA20519, NA18519, HG00126, NA19058, NA19746, HG01067, HG00312, HG00327, NA18964, HG00313, HG00152, HG00734, HG01359, HG00536, NA12750, NA20522, NA20278, HG00344, HG01052, NA18561, NA20506, NA07056, NA18874, HG00731, NA19783, NA20508, NA19060, NA19003, HG01098, NA06989, NA20299, NA20294, NA19670, NA11931
Known GenesZFP14
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv638e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss305
Observed Complex0
Frequencyn/a


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