A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617806



Internal ID7004691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81883225..81907487hg38UCSC Ensembl
Innerchr8:81883225..81907487hg38UCSC Ensembl
Outerchr8:81882725..81907987hg38UCSC Ensembl
chr8:82795460..82819722hg19UCSC Ensembl
Innerchr8:82795460..82819722hg19UCSC Ensembl
Outerchr8:82794960..82820222hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3824263
hg1924263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13240480
SamplesNA20905
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617806
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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