A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv905216



Internal ID6267143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3613004..3718848hg19UCSC Ensembl
Outerchr16:3589110..3730578hg19UCSC Ensembl
Innerchr16:3553005..3658849hg18UCSC Ensembl
Outerchr16:3529111..3670579hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1530829
SamplesMS10311
Known GenesDNASE1, NLRC3, SLX4, TRAP1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv905216
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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