A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22826



Internal ID15497015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61854832..61875414hg38UCSC Ensembl
Outerchr9:61838643..61875898hg38UCSC Ensembl
Innerchr9:67772862..67793437hg19UCSC Ensembl
Outerchr9:67772378..67809632hg19UCSC Ensembl
Innerchr9:67362682..67383257hg18UCSC Ensembl
Outerchr9:67362198..67399452hg18UCSC Ensembl
Innerchr9:66263027..66283602hg17UCSC Ensembl
Outerchr9:66262543..66299797hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3837256
hg1937255
hg1837255
hg1737255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8503
Supporting Variants
SamplesNA19221
Known GenesFAM27B, FAM27E3
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)nssv22826
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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