A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20191



Internal ID15844641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83832521..83833422hg38UCSC Ensembl
Outerchr9:83831662..83834507hg38UCSC Ensembl
Innerchr9:86447436..86448337hg19UCSC Ensembl
Outerchr9:86446577..86449422hg19UCSC Ensembl
Innerchr9:85637256..85638157hg18UCSC Ensembl
Outerchr9:85636397..85639242hg18UCSC Ensembl
Innerchr9:83676990..83677891hg17UCSC Ensembl
Outerchr9:83676131..83678976hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg382846
hg192846
hg182846
hg172846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8539
Supporting Variants
SamplesNA19240
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)nssv20191
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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