A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675099



Internal ID9941204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151708427..151710026hg38UCSC Ensembl
chrX:150876899..150878498hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5509872, essv5802238, essv6505168, essv6411538, essv5477880, essv5957072, essv6506506, essv6177651, essv5650062, essv6470725, essv6040084, essv5529850, essv5692927, essv6490921, essv6319555, essv5661536, essv5696415, essv6246453, essv6190904, essv6004669, essv5641887, essv5534233, essv6541366, essv5661188, essv5748021, essv5795540, essv6334895, essv6061600, essv6015822, essv6197319, essv6498528, essv5748257, essv5578065, essv5901013, essv6303830, essv5818714, essv6362782, essv5958293, essv6090903, essv6248383, essv5831912, essv5693825, essv6173788, essv6464830, essv6408669, essv5783112, essv6381869, essv5898885, essv6185552, essv5575650, essv6223675, essv5977874, essv6028050, essv5794962, essv6575696, essv6488234, essv5597598, essv6357540, essv6142547, essv6518419, essv5741432, essv6344041, essv5728235, essv6510761, essv5693989, essv5571983
SamplesNA19701, NA19703, NA11829, NA18861, NA10851, NA18603, NA12045, NA19350, NA18486, NA18959, NA19098, NA18510, NA12750, NA12155, NA19374, NA19381, NA19373, NA19171, NA19005, NA18940, NA18558, NA18960, NA11992, NA19138, NA11994, NA19207, NA18520, NA19239, NA19445, NA19921, NA19200, NA11993, NA11831, NA18605, NA12003, NA18516, NA18910, NA11919, NA18856, NA19453, HG01101, NA18853, NA19257, NA12144, NA19160, NA18945, NA18974, NA12043, NA18608, NA18953, NA12716, NA11881, NA18961, NA07051, NA19311, NA18943, NA06986, NA19818, NA06994, NA18971, NA19438, NA19093, NA18609, NA18511, NA18522, NA12154
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675099
Frequency
Sample Size1151
Observed Gain0
Observed Loss66
Observed Complex0
Frequencyn/a


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