A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620962



Internal ID7007832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86654855..86671736hg38UCSC Ensembl
chr9:89269770..89286651hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3816882
hg1916882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13546856
SamplesHG02090
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620962
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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