A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16720



Internal ID15831786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65218603..65254018hg38UCSC Ensembl
Outerchr9:65217290..65254489hg38UCSC Ensembl
Innerchr9:70362632..70398102hg19UCSC Ensembl
Outerchr9:70361319..70398574hg19UCSC Ensembl
Innerchr9:69602452..69637922hg18UCSC Ensembl
Outerchr9:69601139..69638394hg18UCSC Ensembl
Innerchr9:67871119..67906589hg17UCSC Ensembl
Outerchr9:67869806..67907061hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3837200
hg1937256
hg1837256
hg1737256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8517
Supporting Variants
SamplesNA12802
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)nssv16720
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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