A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20211



Internal ID15838436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38884422..38886155hg38UCSC Ensembl
Outerchr9:38878208..38886629hg38UCSC Ensembl
Innerchr9:38884419..38886152hg19UCSC Ensembl
Outerchr9:38878205..38886626hg19UCSC Ensembl
Innerchr9:38874419..38876152hg18UCSC Ensembl
Outerchr9:38868205..38876626hg18UCSC Ensembl
Innerchr9:38874419..38876152hg17UCSC Ensembl
Outerchr9:38868205..38876626hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg388422
hg198422
hg188422
hg178422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8446
Supporting Variants
SamplesNA18860
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)nssv20211
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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