A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661218



Internal ID9927323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111198..133111889hg38UCSC Ensembl
Outerchr10:133111161..133111939hg38UCSC Ensembl
Innerchr10:134924702..134925393hg19UCSC Ensembl
Outerchr10:134924665..134925443hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38779
hg19779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv179e199
Supporting Variantsessv6169334, essv5952963, essv5475827, essv6153260, essv6195900, essv5736277, essv5506406, essv6120855, essv5700586, essv6348734, essv6411218, essv5681223, essv6370240, essv6064011, essv6182626, essv5452706, essv6081998, essv6101171, essv6135979, essv6152878, essv5903503, essv6467507, essv6533308, essv6582415, essv6418002, essv5709752, essv6490504, essv6072041, essv6490715, essv5608798, essv6566118, essv6516474, essv6128401, essv5826482, essv5465721, essv5526360, essv5788253, essv6304624, essv6202048, essv6520818, essv6542167, essv5638438, essv5968154, essv6322586, essv6082860, essv5968609, essv6558746, essv6317391, essv5553704, essv6351507, essv5963726, essv6345169, essv5578806, essv5569491, essv6108766, essv5827639, essv5682215, essv5770600, essv5637970, essv6155909, essv5928967, essv5686148, essv6248020, essv6155903, essv5668918, essv6268812, essv6268457, essv5481095, essv6216541, essv5442647, essv5701857, essv6472926, essv5948248, essv6466970, essv5743118, essv6215816, essv6367010
SamplesHG01060, HG00650, NA18565, NA18561, HG00699, NA18545, NA18596, NA18530, NA18606, HG01461, HG00693, NA18988, HG00337, HG00663, HG00501, NA18595, HG00448, NA19457, NA19313, NA19088, NA19681, NA19079, NA18611, HG01072, NA19172, NA19471, NA19087, HG00427, HG00159, NA19445, HG00530, HG00464, NA19007, NA19657, HG00443, HG01171, NA18934, HG00328, HG00732, HG00577, HG00701, HG00657, NA19717, NA19455, NA20314, HG00584, NA18579, NA18534, HG00708, NA18566, HG00613, NA18523, HG00463, NA19318, NA19625, NA20799, NA18542, HG00285, NA19834, NA18961, NA18543, NA19749, NA18950, NA19083, HG00418, HG00672, NA19060, HG00421, NA19468, NA18609, HG00698, NA19430, NA19004, NA18612, NA19429, HG00553, HG00581
Known GenesGPR123
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661218
Frequency
Sample Size1151
Observed Gain0
Observed Loss77
Observed Complex0
Frequencyn/a


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