A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv637e199

Internal ID20123939
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35360143..35372805hg38UCSC Ensembl
chr19:35851045..35863707hg19UCSC Ensembl
Allele length
AssemblyAllele length
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
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)dgv637e199
Sample Size1151
Observed Gain0
Observed Loss217
Observed Complex0

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