A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13147675



Internal ID6343703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25654477..25738502hg38UCSC Ensembl
chr8:25511993..25596018hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3884026
hg1984026
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616687
Supporting Variants
SamplesNA20274
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13147675
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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