A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22254



Internal ID15840145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28781520..28811114hg38UCSC Ensembl
Outerchr16:28779385..28813501hg38UCSC Ensembl
Innerchr16:28792841..28822435hg19UCSC Ensembl
Outerchr16:28790706..28824822hg19UCSC Ensembl
Innerchr16:28700342..28729936hg18UCSC Ensembl
Outerchr16:28698207..28732323hg18UCSC Ensembl
Innerchr16:28700342..28729936hg17UCSC Ensembl
Outerchr16:28698207..28732323hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3834117
hg1934117
hg1834117
hg1734117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9420
Supporting Variants
SamplesNA18975
Known Genes
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)nssv22254
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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