A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662724



Internal ID9928829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70221115..70222736hg38UCSC Ensembl
chr14:70687832..70689453hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381622
hg191622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5451619, essv6309999, essv5502130, essv5605669, essv5418463, essv5643058, essv6570705, essv5465289, essv5733125, essv5767764, essv6525075, essv5433976, essv5965322, essv6188089, essv6308114, essv6132165, essv5672324, essv6382079, essv5581738, essv6457912, essv5925521, essv6016582, essv5741189, essv6503210, essv6483995, essv6113576, essv5418197, essv6588945, essv6335495, essv5733834, essv5414041, essv5834296, essv5419871, essv6340007, essv6516547, essv5569791, essv5466304, essv5471551, essv5560003, essv6256770, essv5960875, essv6131730, essv5915559, essv5449312, essv6212260, essv5541756, essv6589574, essv5829406, essv5476315, essv5583599, essv5909073, essv5464695, essv6122579, essv5983322, essv5557745, essv5912182, essv5631116, essv6007103, essv6447690, essv6279720, essv6588528, essv5820906, essv6363526, essv6170612, essv6508147, essv6549361, essv5456063, essv6475772, essv5512828, essv5695794, essv6128860, essv6144474, essv5996102, essv6276255, essv5724484, essv6550893, essv6330561, essv6119489, essv5988269, essv5955086
SamplesHG00189, NA12717, NA11830, NA12842, HG00143, HG00142, HG00249, HG00242, NA12414, NA12843, NA11933, NA20816, NA20802, NA12045, HG00318, HG00244, HG00181, NA12058, HG00179, HG01518, NA20814, HG01250, HG00127, HG01350, HG01366, HG00272, HG01167, NA12891, NA20769, NA11992, HG01354, HG00311, HG00262, NA12044, HG00160, HG00637, NA20753, HG00313, HG00133, HG01136, NA20535, NA12489, HG00266, HG00176, HG01187, HG00145, NA12878, HG00190, NA20810, NA20314, HG00275, NA12718, HG00740, NA11919, HG00250, NA20581, HG01197, NA11894, NA19750, NA06989, HG00141, NA19685, NA20801, HG00254, HG00278, NA20520, HG01113, HG00319, HG00116, NA07037, HG01489, HG00329, NA12749, HG00342, NA20826, NA19711, NA19661, NA11892, NA18522, HG00554
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662724
Frequency
Sample Size1151
Observed Gain0
Observed Loss80
Observed Complex0
Frequencyn/a


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