A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658667



Internal ID9924772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121010503..121029109hg38UCSC Ensembl
Outerchr10:121010132..121029479hg38UCSC Ensembl
Innerchr10:122770016..122788622hg19UCSC Ensembl
Outerchr10:122769645..122788992hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3819348
hg1919348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv171e199
Supporting Variantsessv5444090, essv6475885, essv5593364, essv6149609, essv6082837, essv5705595, essv6036118, essv6318298, essv5738082, essv6339236, essv5760960, essv5860382, essv5753428, essv5846582, essv5633339, essv6224826, essv6206680, essv5719679, essv5799398, essv6412596, essv5614761, essv6413213, essv5874883
SamplesNA18924, NA18870, NA19171, NA19131, NA18916, NA19197, NA18874, NA19172, NA19189, NA18867, NA19247, NA18933, NA18516, NA18853, NA19099, NA19257, NA18909, NA19108, NA19256, NA19248, NA19102, NA18511, NA18487
Known GenesMIR5694
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658667
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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