A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669974



Internal ID9936079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32713130..32731785hg38UCSC Ensembl
chr9:32713128..32731783hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3818656
hg1918656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1334e199
Supporting Variantsessv6011147, essv5798984, essv5550415, essv5519230, essv5588704, essv6264785, essv6129917, essv6387580, essv6479073, essv5497049, essv6012560, essv6457311, essv5434258, essv5885805, essv6145670, essv5430308, essv6124148, essv5498989, essv5723857, essv6182004, essv6399720, essv6388850, essv5928412, essv6058547, essv5698421, essv6331137, essv5720276, essv5995334, essv5603705, essv5663588, essv6361837, essv5850339, essv6499223, essv6094610, essv5473075, essv5977438, essv5510480, essv5564497, essv5681359, essv5687772, essv5904844, essv6130426, essv6072512, essv5837567, essv5614772, essv5562864, essv5545077, essv5433270, essv5573527, essv6409461, essv6473551, essv5489016, essv6278174, essv6287535, essv6479284, essv5756307, essv5595718, essv5697151, essv5606727, essv6236223, essv5518252, essv6336641, essv6184576, essv6279937, essv6163958, essv5894821, essv5714480, essv6591610, essv5560959
SamplesHG00626, NA19701, HG00650, HG01173, NA19397, NA12273, HG00187, HG01188, HG01066, HG00699, NA18616, HG01140, HG00693, NA19076, HG01366, HG01070, HG00689, HG01354, HG01083, HG00247, HG00335, NA20819, HG00705, HG00182, NA19002, HG01133, HG00178, HG00464, HG01124, HG00313, HG01136, HG00176, HG00282, NA19077, HG00584, HG00533, HG00692, HG01390, HG00324, HG00284, HG01073, HG01334, HG00704, HG00463, NA19469, NA18634, NA19685, HG00285, HG00265, HG00565, NA18628, HG00734, NA19435, NA19010, HG00116, HG01108, HG00662, HG00418, HG00620, HG00614, NA18631, NA19474, HG00174, NA20786, HG00112, HG00698, HG00372, HG00171, HG01191
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669974
Frequency
Sample Size1151
Observed Gain0
Observed Loss69
Observed Complex0
Frequencyn/a


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