A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17794



Internal ID15828601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69403728..69412908hg38UCSC Ensembl
Outerchr9:69402808..69413174hg38UCSC Ensembl
Innerchr9:72018644..72027824hg19UCSC Ensembl
Outerchr9:72017724..72028090hg19UCSC Ensembl
Innerchr9:71208464..71217644hg18UCSC Ensembl
Outerchr9:71207544..71217910hg18UCSC Ensembl
Innerchr9:69248198..69257378hg17UCSC Ensembl
Outerchr9:69247278..69257644hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3810367
hg1910367
hg1810367
hg1710367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8522
Supporting Variants
SamplesNA10839
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)nssv17794
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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