A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13579218



Internal ID6828190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99084600..99098835hg38UCSC Ensembl
chr9:101846882..101861117hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3814236
hg1914236
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621219
Supporting Variants
SamplesNA20902
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13579218
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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