A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv514898



Internal ID15466532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36350230..36355994hg38UCSC Ensembl
Innerchr19:36841132..36846896hg19UCSC Ensembl
Innerchr19:41532972..41538736hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg385765
hg195765
hg185765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2842944, nssv2842938, nssv2842931, nssv2841786, nssv2841814, nssv2841800, nssv2841792, nssv2841738, nssv2841809, nssv2841763, nssv2841815, nssv2841730, nssv2842949, nssv2841736, nssv2841753, nssv2841742, nssv2841783, nssv2842923, nssv2841758, nssv2841799, nssv2841808, nssv2841812, nssv2841789, nssv2842948, nssv2842951, nssv2841757, nssv2841774, nssv2842940, nssv2842927, nssv2841746, nssv2841787, nssv2842956, nssv2841743, nssv2841779, nssv2842935, nssv2841768, nssv2841748, nssv2841745, nssv2841761, nssv2841790, nssv2841785, nssv2842926, nssv2841769, nssv2842932, nssv2841728, nssv2841782, nssv2842953, nssv2841772, nssv2841791, nssv2841729, nssv2841739, nssv2841773, nssv2842933, nssv2841764, nssv2841803, nssv2841797, nssv2841735, nssv2841750, nssv2841737, nssv2842930, nssv2842939, nssv2842937, nssv2842946, nssv2841795, nssv2841765, nssv2842924, nssv2841810, nssv2841751, nssv2841733, nssv2842943, nssv2841798, nssv2841776, nssv2842955, nssv2841754, nssv2841777, nssv2842928, nssv2842947, nssv2841741, nssv2841747, nssv2841770, nssv2841744, nssv2841807, nssv2842929, nssv2841752, nssv2841771, nssv2841760, nssv2841734, nssv2841793, nssv2841755, nssv2841788, nssv2841740, nssv2841804, nssv2842954, nssv2841731, nssv2841801, nssv2842952, nssv2841780, nssv2842936, nssv2841811, nssv2841802, nssv2841813, nssv2842957, nssv2841794, nssv2841806, nssv2841781, nssv2841756, nssv2842958, nssv2841778, nssv2841805, nssv2842950, nssv2841749, nssv2841759, nssv2841732, nssv2842942, nssv2842925, nssv2841762, nssv2841766, nssv2842934, nssv2841796, nssv2841784, nssv2841767, nssv2842941, nssv2842945, nssv2841775
SamplesNA10859, NA12767, NA18964, NA19248, NA19194, NA12750, NA19214, NA12344, NA18594, NA19192, NA21524, NA12802, NA12286, NA18933, NA12801, NA07056, NA18874, NA19173, NA21478, NA19209, NA21447, NA19003, NA21600, NA19223, NA06989, NA12815, NA10847, NA21718, NA06993, NA18947, NA18573, NA07019, NA18484, NA07348, NA12776, NA11893, NA18524, NA18965, NA18488, NA19236, NA18862, NA18868, NA11882, NA11919, NA19211, NA18624, NA12056, NA12282, NA18854, NA18635, NA21716, NA12864, NA07357, NA12873, NA12343, NA12814, NA12740, NA18592, NA19096, NA12761, NA10852, NA18497, NA11843, NA12329, NA18637, NA12777, NA18970, NA19247, NA12239, NA12708, NA07346, NA18518, NA19122, NA19172, NA07014, NA12892, NA19103, NA12778, NA19206, NA12348, NA18498, NA19102, NA06986, NA18875, NA12872, NA21485, NA18978, NA11892, NA18487, NA18564, NA18961, NA18925, NA18997, NA19221, NA19159, NA18974, NA21440, NA18987, NA10851, NA12146, NA18909, NA06984, NA21601, NA12812, NA19123, NA18971, NA19097, NA21480, NA18577, NA12878, NA12546, NA21583, NA18924, NA12045, NA19095, NA10840, NA19171, NA18853, NA18935, NA19249, NA06994, NA18555, NA18519, NA07031
Known GenesZFP14
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv514898
Frequency
Sample Size2366
Observed Gain0
Observed Loss124
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer