A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13415059



Internal ID6631982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17997361..18281756hg38UCSC Ensembl
chr9:17997359..18281754hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38284396
hg19284396
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619862
Supporting Variants
SamplesNA20795
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13415059
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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