A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18579



Internal ID15831014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41341238..41360525hg38UCSC Ensembl
Outerchr9:41341152..41360767hg38UCSC Ensembl
Innerchr9:45424261..45443548hg19UCSC Ensembl
Outerchr9:45424175..45443790hg19UCSC Ensembl
Innerchr9:45314257..45333544hg18UCSC Ensembl
Outerchr9:45314171..45333786hg18UCSC Ensembl
Innerchr9:44363197..44382484hg17UCSC Ensembl
Outerchr9:44363111..44382726hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3819616
hg1919616
hg1819616
hg1719616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8472
Supporting Variants
SamplesNA12740
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)nssv18579
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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