A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9361



Internal ID15500587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:15710129..15719821hg38UCSC Ensembl
Outerchr16:15803986..15813678hg19UCSC Ensembl
Outerchr16:15711487..15721179hg18UCSC Ensembl
Outerchr16:15711487..15721179hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg389693
hg199693
hg189693
hg179693
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27718, nssv26405
SamplesNA18502, NA19221
Known GenesMYH11, NDE1
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)nsv9361
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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