A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21237



Internal ID15841648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40162379..40195367hg38UCSC Ensembl
Outerchr9:40159831..40202967hg38UCSC Ensembl
Innerchr9:43161584..43194424hg19UCSC Ensembl
Outerchr9:43153944..43196972hg19UCSC Ensembl
Innerchr9:43151580..43184420hg18UCSC Ensembl
Outerchr9:43143940..43186968hg18UCSC Ensembl
Innerchr9:45457675..45490663hg17UCSC Ensembl
Outerchr9:45455127..45498263hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3843137
hg1943029
hg1843029
hg1743137
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8483
Supporting Variants
SamplesNA19132
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)nssv21237
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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