A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624234



Internal ID7011090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93099556..93110258hg38UCSC Ensembl
Innerchr10:93100056..93109758hg38UCSC Ensembl
Outerchr10:93098556..93111258hg38UCSC Ensembl
chr10:94859313..94870015hg19UCSC Ensembl
Innerchr10:94859813..94869515hg19UCSC Ensembl
Outerchr10:94858313..94871015hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3810703
hg1910703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13899282, essv13899276, essv13899286, essv13899283, essv13899288, essv13899279, essv13899277, essv13899278, essv13899281, essv13899275, essv13899284, essv13899287, essv13899285, essv13899280
SamplesHG04096, HG03717, HG02691, NA21115, HG03861, HG03786, HG03636, HG04200, NA21143, HG04025, NA21117, HG04239, HG02654, HG04056
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624234
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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