A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25734



Internal ID15487101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33620900..33625488hg38UCSC Ensembl
Outerchr16:33620470..33625819hg38UCSC Ensembl
Innerchr16:33423367..33427955hg19UCSC Ensembl
Outerchr16:33422937..33428286hg19UCSC Ensembl
Innerchr16:33330868..33335456hg18UCSC Ensembl
Outerchr16:33330438..33335787hg18UCSC Ensembl
Innerchr16:33330868..33335456hg17UCSC Ensembl
Outerchr16:33330438..33335787hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg385350
hg195350
hg185350
hg175350
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18504
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)nssv25734
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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