A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672284



Internal ID9938389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107363690..107373246hg38UCSC Ensembl
Outerchr11:107363269..107373666hg38UCSC Ensembl
Innerchr11:107234416..107243972hg19UCSC Ensembl
Outerchr11:107233995..107244392hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3810398
hg1910398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv239e199
Supporting Variantsessv5989195, essv6442543, essv5449408, essv6215924, essv5634668, essv6041198, essv6479312, essv6095583, essv6178630, essv5739319, essv5654251, essv5795708, essv5620335, essv6027546, essv5777784, essv5777300, essv5442462, essv5611238, essv5798606, essv5689692, essv6534051, essv6540054, essv6241302, essv6416745, essv6515446, essv6136672, essv6179050, essv6490774, essv5662166, essv5517223, essv6351096, essv5964418, essv6378764, essv5768084, essv6299715, essv5571826, essv6167344, essv5627733, essv6346078, essv5631065, essv6204174, essv6171080, essv5408392, essv5745139, essv5865235, essv5424856, essv5672118, essv6080253, essv5874474, essv6485919, essv5982724, essv5653364, essv6412993, essv6518172, essv6499691, essv5573680, essv5629409, essv6062066, essv6532481, essv6154956, essv6407908, essv6514111, essv6257822, essv5651859, essv6083921, essv5939559, essv6534770, essv5615861, essv5744168, essv5906280, essv5837532, essv6169224, essv6412464, essv5407007, essv6194137, essv5449779, essv5870360, essv5790920, essv5814330, essv6086265
SamplesNA18502, NA18924, NA19204, NA18861, NA18592, NA18508, NA18507, NA18917, NA18486, NA18596, NA19190, NA19098, NA18870, NA18526, NA18633, NA18510, NA19107, NA18563, NA18550, NA18597, NA18489, NA19119, NA19198, NA18547, NA19131, NA18916, NA18574, NA19197, NA18582, NA18498, NA18874, NA18868, NA19137, NA18520, NA19209, NA18908, NA18539, NA19200, NA19247, NA19152, NA18933, NA19236, NA18637, NA18910, NA18871, NA18572, NA18534, NA18548, NA18907, NA18566, NA18626, NA18856, NA18532, NA18853, NA18553, NA19257, NA18555, NA18523, NA18858, NA18593, NA18576, NA18546, NA18535, NA19108, NA19147, NA18517, NA18501, NA19248, NA19093, NA18609, NA19102, NA18873, NA19213, NA18624, NA18623, NA18522, NA18612, NA18549, NA19153, NA18620
Known GenesCWF19L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672284
Frequency
Sample Size1151
Observed Gain0
Observed Loss80
Observed Complex0
Frequencyn/a


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