A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516537



Internal ID15443830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65869903..65871104hg38UCSC Ensembl
Innerchr16:65903806..65905007hg19UCSC Ensembl
Innerchr16:64461307..64462508hg18UCSC Ensembl
Innerchr16:64461307..64462508hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381202
hg191202
hg181202
hg171202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668986, nssv663643
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516537
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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