A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618883



Internal ID6659077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132868011..132876187hg38UCSC Ensembl
Innerchr8:132868511..132875687hg38UCSC Ensembl
Outerchr8:132867011..132877187hg38UCSC Ensembl
chr8:133880256..133888432hg19UCSC Ensembl
Innerchr8:133880756..133887932hg19UCSC Ensembl
Outerchr8:133879256..133889432hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg388177
hg198177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13338080
SamplesHG03559
Known GenesTG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618883
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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