A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117



Internal ID15489230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39316012..39355151hg38UCSC Ensembl
Outerchr9:39314103..39355467hg38UCSC Ensembl
Innerchr9:39316009..39355148hg19UCSC Ensembl
Outerchr9:39314100..39355464hg19UCSC Ensembl
Innerchr9:39306009..39345148hg18UCSC Ensembl
Outerchr9:39304100..39345464hg18UCSC Ensembl
Innerchr9:39306009..39345148hg17UCSC Ensembl
Outerchr9:39304100..39345464hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3841365
hg1941365
hg1841365
hg1741365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8450
Supporting Variants
SamplesNA18563
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)nssv17117
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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