A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618369



Internal ID7005251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109198080..109224218hg38UCSC Ensembl
chr8:110210309..110236447hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3826139
hg1926139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13283014, essv13283012, essv13283013
SamplesHG03224, NA19917, HG02855
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618369
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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