A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522658



Internal ID15449951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69235288..69244032hg38UCSC Ensembl
Innerchr18:66902525..66911269hg19UCSC Ensembl
Innerchr18:65053505..65062249hg18UCSC Ensembl
Innerchr18:65053505..65062249hg17UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg388745
hg198745
hg188745
hg178745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706060
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522658
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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