A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22670



Internal ID15491185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32178991..32230074hg38UCSC Ensembl
Outerchr16:32178692..32230868hg38UCSC Ensembl
Innerchr16:32190312..32241395hg19UCSC Ensembl
Outerchr16:32190013..32242189hg19UCSC Ensembl
Innerchr16:32097813..32148896hg18UCSC Ensembl
Outerchr16:32097514..32149690hg18UCSC Ensembl
Innerchr16:32097813..32148896hg17UCSC Ensembl
Outerchr16:32097514..32149690hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3852177
hg1952177
hg1852177
hg1752177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18853
Known Genes
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)nssv22670
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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