A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618387



Internal ID7005269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:110028730..110035624hg38UCSC Ensembl
chr8:111040959..111047853hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg386895
hg196895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13285670, essv13285669, essv13285668, essv13285671
SamplesHG02277, HG00355, NA19031, NA18643
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618387
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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