A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520209



Internal ID15447502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11557162..11564906hg38UCSC Ensembl
Innerchr18:11557161..11564905hg19UCSC Ensembl
Innerchr18:11547161..11554905hg18UCSC Ensembl
Innerchr18:11547161..11554905hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg387745
hg197745
hg187745
hg177745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697282
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520209
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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