A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17965



Internal ID15840763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76992979..77002115hg38UCSC Ensembl
Outerchr9:76992421..77002717hg38UCSC Ensembl
Innerchr9:79607895..79617031hg19UCSC Ensembl
Outerchr9:79607337..79617633hg19UCSC Ensembl
Innerchr9:78797715..78806851hg18UCSC Ensembl
Outerchr9:78797157..78807453hg18UCSC Ensembl
Innerchr9:76837449..76846585hg17UCSC Ensembl
Outerchr9:76836891..76847187hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3810297
hg1910297
hg1810297
hg1710297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8529
Supporting Variants
SamplesNA18980
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)nssv17965
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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