A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622322



Internal ID7009181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10091032..10124315hg38UCSC Ensembl
Innerchr10:10091053..10124295hg38UCSC Ensembl
Outerchr10:10091012..10124336hg38UCSC Ensembl
chr10:10132995..10166278hg19UCSC Ensembl
Innerchr10:10133016..10166258hg19UCSC Ensembl
Outerchr10:10132975..10166299hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3833284
hg1933284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv96e214
Supporting Variantsessv13695231
SamplesHG00309
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622322
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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