A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23606



Internal ID15835322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74328419..74430302hg38UCSC Ensembl
Outerchr16:74326758..74431248hg38UCSC Ensembl
Innerchr16:74362317..74464200hg19UCSC Ensembl
Outerchr16:74360656..74465146hg19UCSC Ensembl
Innerchr16:72919818..73021701hg18UCSC Ensembl
Outerchr16:72918157..73022647hg18UCSC Ensembl
Innerchr16:72919818..73021701hg17UCSC Ensembl
Outerchr16:72918157..73022647hg17UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg38104491
hg19104491
hg18104491
hg17104491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9457
Supporting Variants
SamplesNA18552
Known GenesCLEC18B, LOC283922
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)nssv23606
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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