A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19542



Internal ID15832809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7434858..7449403hg38UCSC Ensembl
Outerchr9:7420218..7450456hg38UCSC Ensembl
Innerchr9:7434858..7449403hg19UCSC Ensembl
Outerchr9:7420218..7450456hg19UCSC Ensembl
Innerchr9:7424858..7439403hg18UCSC Ensembl
Outerchr9:7410218..7440456hg18UCSC Ensembl
Innerchr9:7424858..7439403hg17UCSC Ensembl
Outerchr9:7410218..7440456hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3830239
hg1930239
hg1830239
hg1730239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8411
Supporting Variants
SamplesNA18502
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)nssv19542
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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