A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2671723

Internal ID9591142
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72139332..72177658hg38UCSC Ensembl
Outerchr11:72139175..72177811hg38UCSC Ensembl
Innerchr11:71850376..71888702hg19UCSC Ensembl
Outerchr11:71850219..71888855hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5663386, essv6199899, essv6305584, essv6129120, essv6189912, essv6205149, essv5954277, essv6132440, essv6422142, essv6578504, essv6582359, essv6266644, essv5495329, essv6538045, essv6031605, essv5724795, essv5515100, essv5612787, essv5840439, essv5746530, essv6167321, essv5829792, essv5679874, essv5431147, essv6366805, essv6233438, essv5569236, essv5476516, essv6343804, essv6020501, essv6179782, essv5987277, essv5432907, essv6289371, essv6582454, essv6208071, essv5480465, essv5793256, essv5937956, essv6314175, essv5756129, essv6392514, essv6411731, essv6228026, essv5792380, essv5439096, essv6480012, essv6583859, essv6114295, essv5595750, essv5494244, essv6578530, essv6312009, essv6532781, essv5440763, essv6040915, essv5555140, essv6234311, essv6235405, essv5589047, essv6065649, essv6346962, essv5787501, essv6165489, essv6305490, essv6187848, essv6351428, essv6440977, essv6309592, essv5586681, essv6517605, essv6099257, essv5673192, essv5895159, essv6536370, essv5977093, essv5682703, essv5440996, essv6488822, essv5607751, essv5607529, essv6413989, essv6165178, essv5828964, essv6458158, essv6498793, essv5620600, essv6144074, essv5450470, essv5844243, essv5412348, essv5986001, essv5566513, essv6263176, essv5656141, essv6403195, essv5783039, essv5687254, essv5614914, essv5921827, essv5458322, essv5820695, essv5948370, essv6476966, essv5515288, essv6331189, essv6064469, essv5960085, essv6385440, essv5506670, essv5659838, essv5623105, essv5994548, essv6049173, essv5921193, essv5672617, essv6399713, essv5996444, essv5555364, essv6047034, essv5793487, essv5713234, essv5586032, essv6097087, essv5820888, essv5660259, essv6414280, essv6441937, essv6352077, essv6449160, essv5987214, essv6329166, essv6375638, essv5810881, essv5560352, essv6570754, essv5398095, essv6415156, essv5874687, essv6539931, essv5663568, essv6455694, essv6338623
SamplesHG01357, NA18964, HG00318, NA11930, HG00182, NA20785, NA12342, NA18952, NA19114, HG00437, HG01342, NA18501, NA19093, NA19783, NA20508, HG00449, HG00310, NA18550, NA18570, HG00261, HG00707, NA18948, HG00657, HG01082, NA18953, NA18517, NA20529, NA18947, HG00542, NA19338, HG00326, NA18608, NA18542, NA19782, HG01350, NA19379, NA18507, HG00683, HG00187, NA07051, HG00331, NA19780, NA20322, NA18505, NA12044, NA19147, NA19776, NA19654, NA19762, HG00543, HG01107, NA18559, NA20585, NA11919, NA12763, NA19982, HG01140, NA19054, NA18627, NA19390, NA19652, NA19068, HG00140, NA07357, HG01061, NA20530, HG00689, NA20754, NA18592, NA18856, HG00330, NA18956, NA19440, NA18547, HG00125, NA11831, NA20520, HG00237, NA18539, HG00436, NA19377, NA07346, NA12046, HG00233, NA20536, NA19373, HG00629, NA18498, NA18986, NA06986, NA18502, NA19731, NA20540, HG01073, HG00501, HG00672, NA19901, HG00282, HG01069, HG00249, NA20818, HG00478, NA19347, HG01060, NA19789, NA18543, NA18940, NA10851, NA12890, HG00427, NA18983, HG00443, NA18599, NA18909, NA19391, HG01334, NA12749, NA06984, NA18538, NA19403, NA18565, HG00448, NA12003, NA18944, HG00708, HG01251, HG00566, HG00251, HG00324, HG00690, HG00442, NA20524, HG00684, NA19758, NA20502, HG00671, NA20517, NA19779, HG00136, NA19065, NA19746, HG01354, HG00327
Known GenesFOLR3
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2671723
Sample Size1151
Observed Gain0
Observed Loss143
Observed Complex0

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