A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621366



Internal ID7008235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105827588..105901294hg38UCSC Ensembl
chr9:108589869..108663575hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3873707
hg1973707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13593288
SamplesNA18941
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621366
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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