A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615784



Internal ID7002672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:362873..384365hg38UCSC Ensembl
chr8:312873..334365hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3821493
hg1921493
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13054196, essv13054198, essv13054199, essv13054197, essv13054200
SamplesHG02536, NA19209, HG02010, NA20520, NA19779
Known GenesFAM87A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615784
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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