A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24671



Internal ID15842293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74397042..74428861hg38UCSC Ensembl
Outerchr16:74396753..74429098hg38UCSC Ensembl
Innerchr16:74430940..74462759hg19UCSC Ensembl
Outerchr16:74430651..74462996hg19UCSC Ensembl
Innerchr16:72988441..73020260hg18UCSC Ensembl
Outerchr16:72988152..73020497hg18UCSC Ensembl
Innerchr16:72988441..73020260hg17UCSC Ensembl
Outerchr16:72988152..73020497hg17UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg3832346
hg1932346
hg1832346
hg1732346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9457
Supporting Variants
SamplesNA19144
Known GenesCLEC18B
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)nssv24671
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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