A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618893



Internal ID7005775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133614647..133632955hg38UCSC Ensembl
chr8:134626890..134645198hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3818309
hg1918309
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13338117
SamplesNA19372
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618893
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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