A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26541



Internal ID15841875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74423277..74428122hg38UCSC Ensembl
Outerchr16:74422474..74428574hg38UCSC Ensembl
Innerchr16:74457175..74462020hg19UCSC Ensembl
Outerchr16:74456372..74462472hg19UCSC Ensembl
Innerchr16:73014676..73019521hg18UCSC Ensembl
Outerchr16:73013873..73019973hg18UCSC Ensembl
Innerchr16:73014676..73019521hg17UCSC Ensembl
Outerchr16:73013873..73019973hg17UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg386101
hg196101
hg186101
hg176101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9457
Supporting Variants
SamplesNA19132
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)nssv26541
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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