A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622284



Internal ID7009143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8238490..8248891hg38UCSC Ensembl
Innerchr10:8238490..8248891hg38UCSC Ensembl
Outerchr10:8237990..8249391hg38UCSC Ensembl
chr10:8280453..8290854hg19UCSC Ensembl
Innerchr10:8280453..8290854hg19UCSC Ensembl
Outerchr10:8279953..8291354hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3810402
hg1910402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13690315
SamplesHG03437
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622284
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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