A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv905209



Internal ID6267136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3257868..3301897hg19UCSC Ensembl
Outerchr16:3254470..3323569hg19UCSC Ensembl
Innerchr16:3197869..3241898hg18UCSC Ensembl
Outerchr16:3194471..3263570hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1589397, nssv1598320, nssv1596574, nssv1595693
SamplesIS40298, IS38349, IS41025, IS40570
Known GenesFLJ39639, MEFV, OR1F1, OR1F2P, ZNF200
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv905209
Frequency
Sample Size6533
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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