A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv905213



Internal ID6267140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3521051..3718848hg19UCSC Ensembl
Outerchr16:3510737..3730578hg19UCSC Ensembl
Innerchr16:3461052..3658849hg18UCSC Ensembl
Outerchr16:3450738..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 Variantsnssv1543682
SamplesMS16153
Known GenesC16orf90, CLUAP1, DNASE1, NAA60, NLRC3, SLX4, TRAP1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv905213
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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