A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621051



Internal ID6661232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90788855..90818333hg38UCSC Ensembl
chr9:93551137..93580615hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3829479
hg1929479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13555504
SamplesHG00371
Known GenesSYK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621051
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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