A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21930



Internal ID15843953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38898829..38924872hg38UCSC Ensembl
Outerchr9:38898538..38925362hg38UCSC Ensembl
Innerchr9:38898826..38924869hg19UCSC Ensembl
Outerchr9:38898535..38925359hg19UCSC Ensembl
Innerchr9:38888826..38914869hg18UCSC Ensembl
Outerchr9:38888535..38915359hg18UCSC Ensembl
Innerchr9:38888826..38914869hg17UCSC Ensembl
Outerchr9:38888535..38915359hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3826825
hg1926825
hg1826825
hg1726825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8446
Supporting Variants
SamplesNA19221
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)nssv21930
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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