A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520088



Internal ID15100695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11433322..11479757hg38UCSC Ensembl
Innerchr16:11527178..11573613hg19UCSC Ensembl
Innerchr16:11434679..11481114hg18UCSC Ensembl
Innerchr16:11434679..11481114hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3846436
hg1946436
hg1846436
hg1746436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661677, nssv660623
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520088
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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