A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018



Internal ID15836580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38909971..38911066hg38UCSC Ensembl
Outerchr9:38909656..38915950hg38UCSC Ensembl
Innerchr9:38909968..38911063hg19UCSC Ensembl
Outerchr9:38909653..38915947hg19UCSC Ensembl
Innerchr9:38899968..38901063hg18UCSC Ensembl
Outerchr9:38899653..38905947hg18UCSC Ensembl
Innerchr9:38899968..38901063hg17UCSC Ensembl
Outerchr9:38899653..38905947hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg386295
hg196295
hg186295
hg176295
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8446
Supporting Variants
SamplesNA18564
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)nssv18018
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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