A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506



Internal ID15835256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:320139..322740hg38UCSC Ensembl
Outerchr9:319952..324255hg38UCSC Ensembl
Innerchr9:320139..322740hg19UCSC Ensembl
Outerchr9:319952..324255hg19UCSC Ensembl
Innerchr9:310139..312740hg18UCSC Ensembl
Outerchr9:309952..314255hg18UCSC Ensembl
Innerchr9:310139..312740hg17UCSC Ensembl
Outerchr9:309952..314255hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg384304
hg194304
hg184304
hg174304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8403
Supporting Variants
SamplesNA18552
Known GenesDOCK8
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)nssv17506
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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