A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21231



Internal ID15837928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129865033..129872961hg38UCSC Ensembl
Outerchr9:129863731..129875800hg38UCSC Ensembl
Innerchr9:132627312..132635240hg19UCSC Ensembl
Outerchr9:132626010..132638079hg19UCSC Ensembl
Innerchr9:131667133..131675061hg18UCSC Ensembl
Outerchr9:131665831..131677900hg18UCSC Ensembl
Innerchr9:129706866..129714794hg17UCSC Ensembl
Outerchr9:129705564..129717633hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3812070
hg1912070
hg1812070
hg1712070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8571
Supporting Variants
SamplesNA18860
Known GenesMIR6855, USP20
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)nssv21231
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer