A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522262



Internal ID15102869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:54717359..54726513hg38UCSC Ensembl
Innerchr18:52384590..52393744hg19UCSC Ensembl
Innerchr18:50535588..50544742hg18UCSC Ensembl
Innerchr18:50535588..50544742hg17UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg389155
hg199155
hg189155
hg179155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694150
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522262
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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