A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624416



Internal ID7011272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103488996..103492610hg38UCSC Ensembl
Innerchr10:103488996..103492610hg38UCSC Ensembl
Outerchr10:103488736..103492829hg38UCSC Ensembl
chr10:105248753..105252367hg19UCSC Ensembl
Innerchr10:105248753..105252367hg19UCSC Ensembl
Outerchr10:105248493..105252586hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg383615
hg193615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13914618, essv13914617
SamplesNA18486, HG02051
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624416
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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