A curated catalogue of human genomic structural variation

Variant Details

Variant: esv3638110

Internal ID6678208
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18557061..18602909hg38UCSC Ensembl
chr16:18568383..18614231hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15397776, essv15397750, essv15397748, essv15397734, essv15397740, essv15397775, essv15397796, essv15397784, essv15397804, essv15397755, essv15397799, essv15397754, essv15397761, essv15397780, essv15397769, essv15397732, essv15397810, essv15397763, essv15397737, essv15397802, essv15397787, essv15397807, essv15397779, essv15397790, essv15397762, essv15397788, essv15397728, essv15397773, essv15397764, essv15397811, essv15397753, essv15397795, essv15397812, essv15397743, essv15397742, essv15397801, essv15397768, essv15397783, essv15397803, essv15397793, essv15397771, essv15397791, essv15397774, essv15397789, essv15397781, essv15397806, essv15397758, essv15397808, essv15397729, essv15397782, essv15397735, essv15397813, essv15397756, essv15397814, essv15397800, essv15397786, essv15397794, essv15397757, essv15397767, essv15397765, essv15397805, essv15397792, essv15397760, essv15397738, essv15397741, essv15397739, essv15397751, essv15397809, essv15397733, essv15397736, essv15397777, essv15397772, essv15397797, essv15397730, essv15397766, essv15397785, essv15397752, essv15397798, essv15397747, essv15397749, essv15397746, essv15397731, essv15397744, essv15397770, essv15397778, essv15397745, essv15397759
SamplesHG02140, HG01878, HG02122, HG00881, HG03121, HG03832, HG02166, HG01241, HG03762, NA18952, HG02023, HG00500, HG02549, HG03066, NA18570, NA18603, NA20296, NA19317, NA21124, HG02029, HG00701, HG02471, HG02389, NA19320, HG03833, HG03485, HG01860, NA18950, HG01840, NA20770, HG02081, NA18979, HG02137, NA20849, HG00759, NA19792, NA18617, NA18641, NA18638, HG00533, HG03520, NA18976, HG03565, NA19681, NA19056, HG01362, HG00584, HG02392, HG01810, NA19395, NA19786, HG02019, HG02185, NA18633, NA20126, HG00629, HG01806, HG03944, HG02502, HG00534, HG00599, HG01805, NA18562, NA19328, HG02072, NA19318, NA18974, HG02395, HG00589, HG02570, NA18987, HG00590, NA19376, NA19078, HG00717, HG02134, HG03925, HG02187, HG00708, HG03077, HG03814, HG00442, HG01102, HG00476, HG00622, HG03777, NA19439
Known GenesABCC6P1, NOMO2
PlatformMultiple platforms
Pubmed ID21293372
Accession Number(s)esv3638110
Sample Size2504
Observed Gain0
Observed Loss87
Observed Complex0

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