A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24758



Internal ID15483953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34012059..34013238hg38UCSC Ensembl
Outerchr16:34006460..34013809hg38UCSC Ensembl
Innerchr16:33814526..33815705hg19UCSC Ensembl
Outerchr16:33808927..33816276hg19UCSC Ensembl
Innerchr16:33722027..33723206hg18UCSC Ensembl
Outerchr16:33716428..33723777hg18UCSC Ensembl
Innerchr16:33722027..33723206hg17UCSC Ensembl
Outerchr16:33716428..33723777hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg387350
hg197350
hg187350
hg177350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA12155
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)nssv24758
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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