A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616158



Internal ID6656355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8904131..8934011hg38UCSC Ensembl
Innerchr8:8904131..8934011hg38UCSC Ensembl
Outerchr8:8903631..8934511hg38UCSC Ensembl
chr8:8761641..8791521hg19UCSC Ensembl
Innerchr8:8761641..8791521hg19UCSC Ensembl
Outerchr8:8761141..8792021hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3829881
hg1929881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13093742
SamplesNA20761
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616158
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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