A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13351059



Internal ID1254384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139008551..139088445hg38UCSC Ensembl
chr8:140020794..140100688hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3879895
hg1979895
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619001
Supporting Variants
SamplesHG01107
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13351059
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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