A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618418



Internal ID7005300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:111102776..111192695hg38UCSC Ensembl
Innerchr8:111102776..111192695hg38UCSC Ensembl
Outerchr8:111102276..111193195hg38UCSC Ensembl
chr8:112115005..112204924hg19UCSC Ensembl
Innerchr8:112115005..112204924hg19UCSC Ensembl
Outerchr8:112114505..112205424hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3889920
hg1989920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13286356
SamplesNA18986
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618418
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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