A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616868



Internal ID7003754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34886980..34892842hg38UCSC Ensembl
Innerchr8:34887030..34892792hg38UCSC Ensembl
Outerchr8:34886930..34892892hg38UCSC Ensembl
chr8:34744498..34750360hg19UCSC Ensembl
Innerchr8:34744548..34750310hg19UCSC Ensembl
Outerchr8:34744448..34750410hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg385863
hg195863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13165846, essv13165847
SamplesHG04107, HG04035
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616868
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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