A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619014



Internal ID7005895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139282411..139318193hg38UCSC Ensembl
chr8:140294654..140330437hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3835783
hg1935784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13351459
SamplesHG01107
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619014
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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