A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16856



Internal ID15841031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:207465..208215hg38UCSC Ensembl
Outerchr9:206524..208994hg38UCSC Ensembl
Innerchr9:207465..208215hg19UCSC Ensembl
Outerchr9:206524..208994hg19UCSC Ensembl
Innerchr9:197465..198215hg18UCSC Ensembl
Outerchr9:196524..198994hg18UCSC Ensembl
Innerchr9:197465..198215hg17UCSC Ensembl
Outerchr9:196524..198994hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg382471
hg192471
hg182471
hg172471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8403
Supporting Variants
SamplesNA19007
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)nssv16856
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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