A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1475e214



Internal ID22757369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66769053..66782333hg38UCSC Ensembl
chr9:43450178..43463455hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3813281
hg1913278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3620468, esv3620469
SamplesHG01746, NA21097, NA12842, HG01054, NA18947, HG01438, NA20508, NA11995, HG01885, HG01348, HG00351, HG04229, HG01079, HG02648, HG03300, NA18979, HG02804, NA12340, NA12058, HG00179, NA20517, HG01632, HG00337, HG00271, NA12813, NA20814, NA20796, HG03770, HG02140, HG00689, NA20795, HG00238, HG00458, NA12348, HG03736, NA11918, HG02374, HG00346, NA12762, NA12287, NA20287, HG00185, HG02816, HG00158, HG03793, HG02281, NA11930, HG00139, NA20759, HG00277, NA20278, NA20775, HG00309, HG00118, HG02946, HG02104, HG00338, HG01771, HG02780, HG00326, HG02882, HG00365, NA20318, NA20753, HG02879, HG00133, HG00188, NA20800, HG03132, HG01867, HG01171, HG00380, NA19006, HG00332, HG01247, HG04162, HG02775, HG01810, HG00533, HG00344, HG04035, HG01077, HG01852, HG04177, HG01161, NA19000, HG00250, NA11893, NA18532, HG04063, NA18555, HG01474, HG01708, HG00099, HG04118, HG00240, HG02330, HG00476, HG03866, HG00155, HG00254, HG00119, HG00336, NA19019, HG00742, HG04239, HG02696, HG02220, HG00375, HG03692, HG01685, NA20351, NA20530, NA20527, HG03850, HG01620, HG02464, NA12874, NA12763, HG02398, NA18971, HG02095, HG03896, HG03849, NA12749, HG02079, HG03684, HG02768, HG01431, HG01464, HG04056, NA12006, HG01672, NA18740, HG01112, HG01578
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1475e214
Frequency
Sample Size2504
Observed Gain136
Observed Loss0
Observed Complex0
Frequencyn/a


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