A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621052



Internal ID6661233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90793616..90813635hg38UCSC Ensembl
chr9:93555898..93575917hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3820020
hg1920020
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13555505
SamplesHG00371
Known GenesSYK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621052
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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