A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520552



Internal ID15447845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:25038388..25038443hg38UCSC Ensembl
Innerchr16:25049709..25049764hg19UCSC Ensembl
Innerchr16:24957210..24957265hg18UCSC Ensembl
Innerchr16:24957210..24957265hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
hg1756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672467, nssv680393
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520552
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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