A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617337



Internal ID7004223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58460848..58466178hg38UCSC Ensembl
Innerchr8:58460877..58466150hg38UCSC Ensembl
Outerchr8:58460820..58466207hg38UCSC Ensembl
chr8:59373407..59378737hg19UCSC Ensembl
Innerchr8:59373436..59378709hg19UCSC Ensembl
Outerchr8:59373379..59378766hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg385331
hg195331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13206210
SamplesNA21088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617337
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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