A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664084



Internal ID9930189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14912971..14913021hg38UCSC Ensembl
Outerchr10:14912814..14913174hg38UCSC Ensembl
Innerchr10:14954970..14955020hg19UCSC Ensembl
Outerchr10:14954813..14955173hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5690645, essv5790188, essv6406872, essv5958102, essv5426140, essv6117812, essv6475868, essv6461728, essv5501344, essv6403256, essv6060571, essv5578105, essv5987749, essv5451828, essv5719494, essv5504402, essv5573719, essv6490231, essv5623051, essv6531298, essv5823398, essv6317342, essv5670196, essv6134035, essv5806164, essv5803527, essv6517688, essv5914434, essv5811500
SamplesNA12842, HG00242, HG01052, HG01188, HG01389, HG00315, NA19377, HG00327, HG00251, NA12283, HG00281, NA19720, HG01080, HG01170, HG00232, HG01048, HG00137, HG01187, NA19663, HG00263, HG01149, HG01102, HG00140, HG00336, HG01174, HG00329, HG00310, HG01377, NA18612
Known GenesDCLRE1C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664084
Frequency
Sample Size1151
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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