A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21177



Internal ID15494953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41656870..41658316hg38UCSC Ensembl
Outerchr9:41656870..41658823hg38UCSC Ensembl
Innerchr9:46126023..46127585hg19UCSC Ensembl
Outerchr9:46125616..46128092hg19UCSC Ensembl
Innerchr9:46016019..46017581hg18UCSC Ensembl
Outerchr9:46015612..46018088hg18UCSC Ensembl
Innerchr9:44678768..44680330hg17UCSC Ensembl
Outerchr9:44678361..44680837hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381954
hg192477
hg182477
hg172477
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8474
Supporting Variants
SamplesNA19132
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)nssv21177
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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