A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv907336



Internal ID6269263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88868252..88879087hg19UCSC Ensembl
Outerchr16:88858602..88880480hg19UCSC Ensembl
Innerchr16:87395753..87406588hg18UCSC Ensembl
Outerchr16:87386103..87407981hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1507863
SamplesSP54725
Known GenesAPRT, CDT1, GALNS
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv907336
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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