A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620957



Internal ID7007827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86413331..86425131hg38UCSC Ensembl
chr9:89028246..89040046hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3811801
hg1911801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13544306, essv13544307
SamplesHG03199, HG04189
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620957
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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