A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26747



Internal ID15832845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74339471..74360210hg38UCSC Ensembl
Outerchr16:74338415..74362433hg38UCSC Ensembl
Innerchr16:74373369..74394108hg19UCSC Ensembl
Outerchr16:74372313..74396331hg19UCSC Ensembl
Innerchr16:72930870..72951609hg18UCSC Ensembl
Outerchr16:72929814..72953832hg18UCSC Ensembl
Innerchr16:72930870..72951609hg17UCSC Ensembl
Outerchr16:72929814..72953832hg17UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg3824019
hg1924019
hg1824019
hg1724019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9457
Supporting Variants
SamplesNA18502
Known GenesLOC283922
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)nssv26747
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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