A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24541



Internal ID15829855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85972649..85974035hg38UCSC Ensembl
Outerchr16:85970578..85974222hg38UCSC Ensembl
Innerchr16:86006255..86007641hg19UCSC Ensembl
Outerchr16:86004184..86007828hg19UCSC Ensembl
Innerchr16:84563756..84565142hg18UCSC Ensembl
Outerchr16:84561685..84565329hg18UCSC Ensembl
Innerchr16:84563756..84565142hg17UCSC Ensembl
Outerchr16:84561685..84565329hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg383645
hg193645
hg183645
hg173645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9467
Supporting Variants
SamplesNA11830
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)nssv24541
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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