A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26780



Internal ID15486138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87987011..87992876hg38UCSC Ensembl
Outerchr16:87986404..87994114hg38UCSC Ensembl
Innerchr16:88020617..88026482hg19UCSC Ensembl
Outerchr16:88020010..88027720hg19UCSC Ensembl
Innerchr16:86578118..86583983hg18UCSC Ensembl
Outerchr16:86577511..86585221hg18UCSC Ensembl
Innerchr16:86578118..86583983hg17UCSC Ensembl
Outerchr16:86577511..86585221hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg387711
hg197711
hg187711
hg177711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9472
Supporting Variants
SamplesNA18502
Known GenesBANP
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)nssv26780
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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