A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643692



Internal ID6683763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12053796..12066895hg38UCSC Ensembl
Innerchr19:12054296..12066395hg38UCSC Ensembl
Outerchr19:12052796..12067895hg38UCSC Ensembl
chr19:12164611..12177710hg19UCSC Ensembl
Innerchr19:12165111..12177210hg19UCSC Ensembl
Outerchr19:12163611..12178710hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3813100
hg1913100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15991905, essv15991922, essv15991936, essv15991912, essv15991907, essv15991915, essv15991879, essv15991920, essv15991898, essv15991890, essv15991897, essv15991900, essv15991910, essv15991931, essv15991913, essv15991884, essv15991876, essv15991902, essv15991888, essv15991939, essv15991908, essv15991937, essv15991924, essv15991941, essv15991918, essv15991926, essv15991892, essv15991917, essv15991881, essv15991894, essv15991885, essv15991935, essv15991914, essv15991916, essv15991899, essv15991895, essv15991934, essv15991880, essv15991886, essv15991877, essv15991940, essv15991929, essv15991903, essv15991932, essv15991901, essv15991909, essv15991921, essv15991891, essv15991893, essv15991919, essv15991930, essv15991887, essv15991923, essv15991911, essv15991883, essv15991896, essv15991933, essv15991889, essv15991882, essv15991878, essv15991938, essv15991927, essv15991904, essv15991925, essv15991906, essv15991928
SamplesHG00403, HG00542, HG00671, NA18647, HG00559, HG01815, HG02029, NA18641, HG02061, NA18603, HG02360, HG01802, NA18625, HG01809, NA18988, HG00717, HG01873, HG02016, HG02087, HG00689, HG00599, NA18582, HG01859, HG02131, HG02389, NA19075, HG02409, NA18645, HG01841, HG02070, HG00596, HG02142, HG02025, HG00657, HG02084, HG00556, HG01845, NA18637, HG01808, HG00708, HG00692, NA19000, HG00844, HG01870, HG02121, HG02141, HG02184, HG00463, HG01596, HG00445, NA19012, NA18542, NA18533, NA18543, HG02088, HG00565, HG00607, NA18629, NA19467, NA18643, HG02139, HG02019, HG01862, HG01801, HG02367, NA19004
Known GenesZNF844
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643692
Frequency
Sample Size2504
Observed Gain0
Observed Loss66
Observed Complex0
Frequencyn/a


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