A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522688



Internal ID15449981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:47354..55444hg38UCSC Ensembl
Innerchr16:97354..105444hg19UCSC Ensembl
Innerchr16:37354..45444hg18UCSC Ensembl
Innerchr16:37354..45444hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388091
hg198091
hg188091
hg178091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706098
Samples
Known GenesPOLR3K, SNRNP25
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522688
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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