A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618222



Internal ID7005105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102433508..102443861hg38UCSC Ensembl
Innerchr8:102434008..102443361hg38UCSC Ensembl
Outerchr8:102432508..102444861hg38UCSC Ensembl
chr8:103445736..103456089hg19UCSC Ensembl
Innerchr8:103446236..103455589hg19UCSC Ensembl
Outerchr8:103444736..103457089hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3810354
hg1910354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13269776, essv13269781, essv13269777, essv13269774, essv13269773, essv13269778, essv13269780, essv13269775, essv13269779
SamplesNA20882, NA20766, NA21127, NA20900, NA21109, HG04035, NA20875, HG03643, NA21088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618222
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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