A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675603



Internal ID9595022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108294671..108299497hg38UCSC Ensembl
chr13:108947019..108951845hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg384827
hg194827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv379e199
Supporting Variantsessv6134156, essv6274448, essv6303769, essv5775007, essv6076658, essv5780003, essv5668470, essv6524377, essv5454531, essv6313563, essv5856539, essv6016711, essv6420661, essv6478583, essv5647855, essv5801501, essv6238569, essv6329877, essv6567497, essv6235612, essv6377256, essv5763254, essv5879928, essv6008265, essv6127065, essv6375117, essv5661915, essv6271307, essv5627748, essv5555651, essv6189788, essv5714018, essv5804630, essv6243316, essv5429785, essv6116003, essv6515895, essv5445797, essv5859643, essv5907883, essv5519788, essv6078511, essv5468917, essv5954758, essv6091694, essv6319386, essv5871815, essv5910924, essv5908746, essv5548092
SamplesNA11830, NA11995, NA18508, NA12273, NA11920, NA11933, NA12045, NA18504, NA12340, NA19098, NA12400, NA12341, NA12813, NA18519, NA18489, NA18923, NA11992, NA19197, NA12283, NA19130, NA18874, NA12044, NA11994, NA19235, NA19159, NA19209, NA18908, NA11993, NA18934, NA19152, NA18871, NA19114, NA11893, NA12249, NA06989, NA12716, NA19108, NA19147, NA18517, NA12775, NA07037, NA06986, NA19248, NA18873, NA19213, NA07056, NA11892, NA18487, NA19153, NA12776
Known GenesTNFSF13B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675603
Frequency
Sample Size1151
Observed Gain0
Observed Loss50
Observed Complex0
Frequencyn/a


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