A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv28077



Internal ID15497146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34005948..34015878hg38UCSC Ensembl
Outerchr16:34005775..34016243hg38UCSC Ensembl
Innerchr16:33808415..33818345hg19UCSC Ensembl
Outerchr16:33808242..33818710hg19UCSC Ensembl
Innerchr16:33715916..33725846hg18UCSC Ensembl
Outerchr16:33715743..33726211hg18UCSC Ensembl
Innerchr16:33715916..33725846hg17UCSC Ensembl
Outerchr16:33715743..33726211hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3810469
hg1910469
hg1810469
hg1710469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA19221
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)nssv28077
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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