A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658884



Internal ID9578303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108294468..108300374hg38UCSC Ensembl
Outerchr13:108294097..108300744hg38UCSC Ensembl
Innerchr13:108946816..108952722hg19UCSC Ensembl
Outerchr13:108946445..108953092hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg386648
hg196648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv379e199
Supporting Variantsessv5870858, essv5765534, essv6014038, essv5617897, essv5939220, essv6359707, essv5851410, essv6071039, essv6404447, essv6493974, essv5614315, essv6243000, essv6576199, essv6060804, essv5583009, essv5776089, essv5919196, essv5699713, essv5883716, essv5651059, essv5487582, essv5495172, essv5852432, essv6011978, essv5957535, essv6283433, essv5547919
SamplesNA19332, NA19350, NA19393, NA19443, NA19379, NA19384, NA19471, NA19451, NA19462, NA19327, NA19455, NA19453, NA19338, NA19452, NA19469, NA19395, NA19436, NA19401, NA19375, NA19440, NA19390, NA19435, NA19439, NA19467, NA19376, NA19430, NA19316
Known GenesTNFSF13B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658884
Frequency
Sample Size1151
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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