A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16535



Internal ID15482495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11318858..11610269hg38UCSC Ensembl
Outerchr9:11173118..11631933hg38UCSC Ensembl
Innerchr9:11318858..11610269hg19UCSC Ensembl
Outerchr9:11173118..11631933hg19UCSC Ensembl
Innerchr9:11308858..11600269hg18UCSC Ensembl
Outerchr9:11163118..11621933hg18UCSC Ensembl
Innerchr9:11308858..11600269hg17UCSC Ensembl
Outerchr9:11163118..11621933hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38458816
hg19458816
hg18458816
hg17458816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8415
Supporting Variants
SamplesNA10847
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)nssv16535
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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