A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv638e199

Internal ID20123940
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36348743..36356170hg38UCSC Ensembl
chr19:36839645..36847072hg19UCSC Ensembl
Allele length
AssemblyAllele length
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
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)dgv638e199
Sample Size1151
Observed Gain0
Observed Loss305
Observed Complex0

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