A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22956



Internal ID15488363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14692501..14704993hg38UCSC Ensembl
Outerchr16:14691443..14707053hg38UCSC Ensembl
Innerchr16:14786358..14798850hg19UCSC Ensembl
Outerchr16:14785300..14800910hg19UCSC Ensembl
Innerchr16:14693859..14706351hg18UCSC Ensembl
Outerchr16:14692801..14708411hg18UCSC Ensembl
Innerchr16:14693859..14706351hg17UCSC Ensembl
Outerchr16:14692801..14708411hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3815611
hg1915611
hg1815611
hg1715611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9353
Supporting Variants
SamplesNA18537
Known GenesPLA2G10
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)nssv22956
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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