A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616416



Internal ID7003303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15889214..15901196hg38UCSC Ensembl
Innerchr8:15889214..15901196hg38UCSC Ensembl
Outerchr8:15888714..15901696hg38UCSC Ensembl
chr8:15746723..15758705hg19UCSC Ensembl
Innerchr8:15746723..15758705hg19UCSC Ensembl
Outerchr8:15746223..15759205hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3811983
hg1911983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13118939, essv13118938
SamplesHG03757, NA18541
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616416
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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