A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618434



Internal ID7005316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:111558218..111710129hg38UCSC Ensembl
chr8:112570447..112722358hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38151912
hg19151912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13288122
SamplesHG02855
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618434
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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