A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9437



Internal ID15847349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:30328019..30335038hg38UCSC Ensembl
Outerchr16:30339340..30346359hg19UCSC Ensembl
Outerchr16:30246841..30253860hg18UCSC Ensembl
Outerchr16:30246841..30253860hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg387020
hg197020
hg187020
hg177020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22930
SamplesNA18564
Known GenesLOC595101
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nsv9437
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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