A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21816



Internal ID15482660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:685891..690468hg38UCSC Ensembl
Outerchr16:684861..690961hg38UCSC Ensembl
Innerchr16:735891..740468hg19UCSC Ensembl
Outerchr16:734861..740961hg19UCSC Ensembl
Innerchr16:675892..680469hg18UCSC Ensembl
Outerchr16:674862..680962hg18UCSC Ensembl
Innerchr16:675892..680469hg17UCSC Ensembl
Outerchr16:674862..680962hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386101
hg196101
hg186101
hg176101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9321
Supporting Variants
SamplesNA10863
Known GenesWDR24
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)nssv21816
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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