A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24334



Internal ID15484124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32562515..32595438hg38UCSC Ensembl
Outerchr16:32481626..32596350hg38UCSC Ensembl
Innerchr16:32573836..32606759hg19UCSC Ensembl
Outerchr16:32492947..32607671hg19UCSC Ensembl
Innerchr16:32481337..32514260hg18UCSC Ensembl
Outerchr16:32400448..32515172hg18UCSC Ensembl
Innerchr16:32481337..32514260hg17UCSC Ensembl
Outerchr16:32400448..32515172hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38114725
hg19114725
hg18114725
hg17114725
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)nssv24334
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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