A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17840



Internal ID15837782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41297390..41318211hg38UCSC Ensembl
Outerchr9:41296972..41318765hg38UCSC Ensembl
Innerchr9:45380413..45401234hg19UCSC Ensembl
Outerchr9:45379995..45401788hg19UCSC Ensembl
Innerchr9:45270409..45291230hg18UCSC Ensembl
Outerchr9:45269991..45291784hg18UCSC Ensembl
Innerchr9:44319349..44340170hg17UCSC Ensembl
Outerchr9:44318931..44340724hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3821794
hg1921794
hg1821794
hg1721794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8472
Supporting Variants
SamplesNA18853
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)nssv17840
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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