A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516117



Internal ID15096724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5235393..5301110hg38UCSC Ensembl
Innerchr16:5285394..5351111hg19UCSC Ensembl
Innerchr16:5225395..5291112hg18UCSC Ensembl
Innerchr16:5225395..5291112hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3865718
hg1965718
hg1865718
hg1765718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668846, nssv666316, nssv686619, nssv688261
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516117
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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