A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv637e199



Internal ID18982691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35360143..35372805hg38UCSC Ensembl
chr19:35851045..35863707hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812663
hg1912663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672319, esv2667130, esv2678346
SamplesHG00323, HG00613, HG01441, NA18621, HG00309, NA12154, NA12249, HG00252, HG00607, HG01440, NA12750, HG00257, NA18595, NA07037, NA18951, NA18534, HG00344, NA18530, NA18630, NA12342, HG00127, HG00328, NA18975, HG01342, HG00171, NA18612, HG00112, HG00596, NA12347, HG00155, HG00160, HG00449, NA19060, HG00310, NA18570, NA19003, HG00707, NA10847, NA12340, NA18545, HG01389, NA18948, HG00657, HG01365, HG00577, NA18953, NA18972, NA12828, HG00428, NA19010, HG00542, HG00326, NA18573, NA18608, HG00148, HG01350, HG00139, NA18541, HG00106, HG00701, NA12776, HG00187, HG00651, HG00366, NA11893, HG00177, HG00146, HG00253, NA12341, NA12287, NA18943, HG00353, HG00247, NA18632, HG00244, HG00154, NA19062, HG00321, HG00158, NA18624, NA18967, HG01456, NA19059, NA12282, NA12383, HG00337, NA11994, NA18635, NA18576, NA18960, HG00259, NA18563, NA18618, HG00096, HG00610, HG00231, HG00692, HG01495, HG00689, NA18636, HG00628, HG00330, NA07048, NA12761, NA18638, NA19066, HG00178, HG00419, NA18547, HG00258, NA11843, NA11831, NA11894, NA19075, HG00264, HG01253, NA11995, HG00174, NA18593, HG00254, HG00276, NA12777, HG00237, HG00343, NA12144, NA19082, NA18539, HG00114, NA12751, HG00436, HG00267, HG00620, NA19080, NA12046, HG00108, NA12716, HG01465, HG00268, NA12778, NA18968, HG00263, NA12275, NA19002, HG00239, NA18941, HG00232, HG01356, HG00249, HG00478, NA18564, NA18961, HG00513, NA18988, HG00512, HG00534, NA12283, NA18562, NA18579, NA18985, HG00236, NA18543, NA18940, NA11832, NA18619, NA18987, NA18582, NA18597, HG00590, HG00595, NA12272, HG00443, NA18599, NA19078, NA06984, NA18538, NA12413, NA18565, NA19009, HG00663, HG00262, NA18631, NA18560, HG01112, HG00118, HG00530, NA11992, NA12003, NA19064, HG00281, HG00285, NA12399, HG00656, NA18610, HG00367, NA12045, NA11932, HG00566, HG01125, HG00119, HG00320, HG01498, HG00275, HG00690, NA12717, NA18532, HG00137, HG00684, HG01377, NA06994, HG00336, HG00704, NA18555, HG00271, NA19007, HG00136, HG00126, HG00327
Known GenesFFAR3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv637e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss217
Observed Complex0
Frequencyn/a


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