A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21862



Internal ID15838875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74330404..74373412hg38UCSC Ensembl
Outerchr16:74329523..74374680hg38UCSC Ensembl
Innerchr16:74364302..74407310hg19UCSC Ensembl
Outerchr16:74363421..74408578hg19UCSC Ensembl
Innerchr16:72921803..72964811hg18UCSC Ensembl
Outerchr16:72920922..72966079hg18UCSC Ensembl
Innerchr16:72921803..72964811hg17UCSC Ensembl
Outerchr16:72920922..72966079hg17UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg3845158
hg1945158
hg1845158
hg1745158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9457
Supporting Variants
SamplesNA18942
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)nssv21862
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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