A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516054



Internal ID15443347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28293676..28322090hg38UCSC Ensembl
Innerchr16:28304997..28333411hg19UCSC Ensembl
Innerchr16:28212498..28240912hg18UCSC Ensembl
Innerchr16:28212498..28240912hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3828415
hg1928415
hg1828415
hg1728415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv666644, nssv659114, nssv691804, nssv689307, nssv665895, nssv691157, nssv691224, nssv689019, nssv666821, nssv692935, nssv682700, nssv681463, nssv688005, nssv670779, nssv674455, nssv684274, nssv659070, nssv672658, nssv677573
Samples
Known GenesSBK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516054
Frequency
Sample Size2026
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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