A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17896



Internal ID15835282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41368575..41380933hg38UCSC Ensembl
Outerchr9:41367441..41381553hg38UCSC Ensembl
Innerchr9:45451598..45463956hg19UCSC Ensembl
Outerchr9:45450464..45464576hg19UCSC Ensembl
Innerchr9:45341594..45353952hg18UCSC Ensembl
Outerchr9:45340460..45354572hg18UCSC Ensembl
Innerchr9:44390534..44402892hg17UCSC Ensembl
Outerchr9:44389400..44403512hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3814113
hg1914113
hg1814113
hg1714113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8472
Supporting Variants
SamplesNA18552
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)nssv17896
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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